[1]United States Patetit Office 315629297 3,562,297 ALKANOLAMINE DERIVATIVE4 S Ralph Howe and Leslie Harold Smith, Macclesfield, England, assignors to Imperial Chemical Indusfties Limited, London, England, a corporation of Great Britain No Drawing. Filed Oct. 16, 1967, Ser. No. 675295 Claims priority, application England, Nov. 3, '6661 49,368/66 Int. Cl. C07c 103130 U.S. Cl. 260-347.3 5 Claims ABSTRACT OF THE DISCLOSURE The disclosure relates to I-acylaminophenoxy-3-amino2-propanot derivatives, processes for their manufacture and pharmaceutical compositions containing them. The said compounds possess p-adrenergic blocking activity and are useful in the treatment of heart diseases. Representative of the compounds disclosed is 1-(4- propionamidophenoxy)-3-isopropylamino-2-propanol. This invention relates to new alkanolamine derivatives which possess 3-adrenergic blocking activity and which are therefore useful in the treatment or prophylaxis of heart diseases, for example angina pectoris and cardiac arrhythmias, and in the treatment of hypertension and phaeochromocytoma, in man. According to the invention we provide new alkanolamine derivatives of the formula: OR4 I OCH2- CH. CH2NHR1 R2CONTT R3 wherein either (a) RI stands for an alkyl radical which may optionally be si-ibstituted by one or more radicals selected from hydroxy and aryl radicals, which aryl radicals may themselves optionally be further substittited by one or more halogen atoms or alkyl or alkoxy radicals, or RI stands for a cycloalkyl or alkenyl radical, R2 stands for hydrogen or for a hydroxyalkyl, aryloxyalkyl, halogenoalkyl, cycloalkyl, heterocyclyl or acylaminophenyl radical, or for the ethyl, vinyl, p-tolyl or m-nitrophenyl radical, R3 stands for hydrogen or for an alkyl radical and R4 stands for hydrogen or for an acyl radical; or (b) R' stands for the methyl or cyclopropyl radical, R2 stands for hydrogen or for an alkyl, alkenyl, aryl, aralkyl or alkoxy radical, R3 stands for hydrogen or for an alkyl radical and R4 stands for hydrogen or for an acyl radical; or (c) R' stands for the isopropyl radical, Rs stands for the methyl radical, R4 stands for hydrogen or for an acyl radical and either R3 stands for hydrogen and the group R2CONH- is in the 2-position relative to the alkanolamine side-chain, or R3 stands for the methyl radical in the 5-position relative to the alkanolamine side-chain and the group R2CONH- is in the 3-position relative to the alkanolamine side-chain, or R3 stands for the methyl radical in the 3-position relative to the alkanolamine sidePatented Feb. 9, 1971 2 chain and the group R2CONH- is in the 4-position relative to -the alkanolamine sidechain, or R3 stands for the n-butyl radical in the 2-position relative to the alkanolamine side-chain and the group R2CONH- is in the 5position relative to the alkanolamine sidechain; or 5 (d) R' stands for the isopropyl radical, R2 stands for -the methyl radical, R3 stands for hydrogen and R4 stands for the acetyl radical; and the acid-addition salts thereof. It is to b.- understood that the above definition of 10 alkanolamine derivatives encompasses all possible stereoisomers thereof, and mixtures thereof. As a suitable value for R' when it stands for an alkyl radical, optionally substituted, there may be mentioned, for example, an alkyl radical of not more than 12 carbon 15 atoms and particularly of 3, 4 or 5 carbon atoms, which preferably is branched at the a-carbon atom, for example the isopropyl, s-butyl or t-butyl radical, which alkyl radical may optionally be substituted by one or two radicals selected from hydroxy radicals and phenyl radicals which 20 may themselves optionally be substituted by one or more chlorine or bromine atoms or methyl, ethyl, methoxy or ethoxy radicals. Thus, a specific value for RI when it stands for an alkyl radical, optionally substituted, is the isopropyl, s-butyl, tbutyl, 2-hydroxy-1,1-dimethylethyl, 25 1-methyl-3-phenylpropyl, 2-(4-methoxyphe nyl)-l-methylethyl or 3-(4- chlorophenyl)-I,I-dimethylpropyl radical. As a suitable value for RI or R2 when it stands for a cycloalkyl radical there may be mentioned, for example, a cycloalkyl radical of not more than 8 carbon atoms, 30 for example the cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl radial. As a suitable value for R' when it stands for an alkenyl radical there may be mentioned, for example, an alkenyl radical of not more than 6 carbon atoms, for example the 35 allyl radical. As a suitable value for R2 when it stands for a hydroxyalkyl, aryloxyalkyl or halogenoalkyl radical there may be mentioned, for example, an alkyl radical of not more than 6 carbon atoms which is substituted by a hydroxy 40 or phenoxy radical or by a chlorine or bromine atom, or by one or more fluorine atoms, for example the hydroxymethyl, phenoxymethyl, chloromethyl or trifluoromethyl radical. As a suitable value for R2 when it stands for a hetero45 cyclyl radical there may be mentioned, for example, a heterocyclyl radical of 5 or 6 ring atoms one or two of which are selected from nitrogen, oxygen and sulphur atoms. A specific value for R2 when it stands for a heterocyclyl radical is, for example, the furyl, thienyl or pyridyl 50 radical. As a suitable value for R2 when it stands for an acylaminophenyl radical there may be mentioned, for example, a phenyl radical substituted by an alkanoylamino or alkanesulphonylamino radical each of not more than 55 6 carbon atoms or an aroylamino or aienesulphonylamino radical each of not more than 10 carbon atoms, for example an acetamidophenyl, methanesulphonamidophenyl, benzamidophenyl or toluene - p - sulphonamidophenyl radical. 60 As a suitable value for R2 when it stands for an alkyl, alkenyl or alkoxy radical there may be mentioned, for example, an alkyl, alkenyl or alkoxy radical each of not more than 6 carbon atoms, for example the methyl, ethyl, vinyl, methoxy or ethoxy radical.
[2]3)562@297 3 As a suitable value for R2 when it stands for an aryl or aralkyl radical there may be mentioned, for example, an aryl or aralkyl radical of not more than 10 carbon atoiiis, for example the phenyl, p-tolyl, p-chlorophenyl or benzyl radical. As a suitable value for R3 when it stands for a alkyl radical there may be mentioned, for example, an alkyl radical of not more than 6 carbon atoms, for example the methyl or ethyl radical. As a suitable value for R4 when it stands for an acyl radical there may be mentioned, for example, an alkanoyl or alkenoyl radical of not more than 20 carboii atoms, for example the acetyl, palmityl, stearyl or oleyl radical, or an aroyl radical o,f not more than 10 carbon atoms, for example the benzoyl radical. As suitable acid-addition salts of the alkanolamine derivatives of the invention there may be mentioned, for example, salts derived from inorganic acids, for example hydrochlorides, hydrobromides, phosphates or sulphates, or salts derived from organic acids, for exan-iple oxalates, lactates, tartrates, acetates, salicylates, citrates, benzoates, p-naphthoates, adipates or 1,1-methylene -bis-(2-hydroxy3-naphthoates), or salts derived from acidic synthetic resins, for examplesulphonated polystyrene resins, for example "Zeo-Karb" 225 ("Zeo-Karb" is a trademark). Specific new alkanolamine derivatives of the invention are, for example, 1- (4-propionamidophenoxy) -3-isopropylamino-2propanol; 1- (5-acetamido-2-n-butylphenoxy) -3-isopropylamino-2propanol; 1-(4-acetamido-3-methylphenoxy)-3-isopropylamino-2- propanol; 1-(4-formamidophenoxy)-3-isopropylamino-2-propanol-I 1-(4-phenoxyacetamidophenoxy)-3-isopropylamino-2- propanol; 1- (4-acetamidophenoxymethyl) -2-isopropylaminoethyl acetate; 1- (2-acetamidophenoxy) -3-isopropylamino-2-propanol; 1- (4-chloroacetamidophenoxy) -3-isopropylamino-2propanol; 1-(4-cyclohexanecarbonamidophenoxy)-3-isopropylamino-2-propanol; 1-(4-hydroxyacetamidophenoxy)-3-isopropylamino-2- propanol; 1-[4-(2-furamido)phenoxy]-3-isopropylamino-2- propanol; 1- (4-cyclopropanecarbonamidophenoxy) -3-isopropyl amino-2-propanol; 1-[4-(p-acetamidobenzamido)phenoxy]-3-isopropylamino-2-propanol; 1-(4-m-nitrobenzamidophenoxy)-3-isopropylamino-2- propanol; 1-(4-p-toluamidophenoxy)-3-isopropylamino-2-propanol; 1-(4-acrylamidophenoxy)-3-isopropylamino-2-propanol; 1-(4-acetamidophenoxy)-3-cyclopropylamino-2- propanol; 1- (4-acetamidophenoxy) -3-methylamino-2-propanol; 1- (3-acetamido-5-methylphenoxy) -3-isopropyamino-2propanol; and 1-(4-propionamidophenoxy)-3-t-butylamino-2-propanol; and the acid-addition salts thereof. According to a further feature of the invention we provide a process for the manufacture of those of the alkanolamine derivatives of the invention wherein R4 stands for hydrogen, and the acid-addition salts thereof, which comprises the interaction of a compound of the formula: C--,\\\,-OC112X R2CO.NH R3 wherein R2 and R3 have the meanings statcd above anit wherein X stands for the group 0 -Cli-CII2 4 or the group -CI40H.CH2y, wherein Y stands for a lialogen atom, or of mixtures of such components wherein X has both meanings stated above, with an amine of the formula NH2R', wherein RI has the meaning stated above, wbei-eafter, if desired, the product in free base form is reacted with an acid in order to form an acid-addition salt. As a suitable value for Y there may be mentioned, for exaniple, a chlorine or bromine atom. The interaction may 10 be carried out at ambient temperature or it may be accelerated or completed by the application of heat, for example by heatin@, to a temperature of 90-110' C.; it may be carried out at atmospheric or at an elevated pressure, for example by heating in a sealed vessel; and 15 it may be carried out in an inert diluent or solvent, for eximple methanol or ethanol, or aR excess of the amine of the formula NH2R', wherein RI has the meaning stated above, may be used as diluent or solvent. The starting material used in the above process may be 20 obtained by the interaction of the corresponding phenol with an epihalohydrin, for example epichlorohydrin. The said starting material may be isolated or it may be prepared and used in situ without isolation. According to a further feature of the invention we pro25 vide a process for the manufacture of those of the alka@nolamine derivatives of the invention wherein R4 stands for hydrogen, and the acid-add;tion salts thereof, which comprises the interaction of a compound of the formula: OCH2.CHOH.CH2NHR1 30 H2N R3 wherein RI and R3 have the meanings stated above, with an acylating agent derived from an acid of the formula 35 R2COOH, wherein R2 has the meaning stated above, under stich conditions that neither the amino nor the hydroxy radical of the alkanolamine side-chain is acylated, whereafter, if desired, the product in free base form is reacted with an acid in order to form an acid-addition 40 salt. Suitable conditions are provided, for example, by the use of an acyl halide, for example an acyl chloride, or acid anhydride in aqueous conditions, for example in water or aqueous acetone, at a pH of between 3 and 7, preferably between 4 and 5, and at ambient temperature. 45 A suitable acylating a.-ent is, for example, acetic anhydride or propionic anhydride. Alternatively, the acylation may be carried out by means of the acid of the formula R2COOH itself in an inert diluent or solvent, for example ethyl acetate, and in 50 the presence of a condensing agent, for example a carbodiimide. The reaction may be carried out at ambient temperature or, preferably, at a reduced temperature, for example at 0-5' C. According to a further feature of the invention we pro55 vide a process for the manufacture of those of the alkanolamine derivatives of the invention wherein RI does not stand for a hydrogenolysable aralkyl group and wherein R4 stands for hydro-en, and the acid-addition salts thereof, which comprise@s the hydrogenolysis of a 60 compound of the formula: \ OCII2CHOH.CH2NRIR5 R2CO.NH R3 65 wherein RI, R2 and R3 have the meanings stated above and wherein R5 stands for a hydrogenolysable radical, or an acid-addition salt thereof, whereafter, if desired, the product in free base form is reacted with an acid in order to form an acidaddition salt. 70 As a stiitable value for R5 there may be mentioned, for example, the benzyl radical. The hydrogenolysis may be effected, for example, by catalytic hydrogenation, for exaniple by hydrogenation in the presence of a pall aditimoii-charcoal catalyst, in an inert di]Lient or solvent, for 75 example ethanol or aqueous ethanol, at ambient temper-
[3]8,562,297 5 ature and at atmospheric pressure or at an elevated pressure, for example at a pressure of 100 atmospheres. The process may be accelerated or completed by the presence of an acidic catalyst, for example hydrochloric or oxalic acid. 5 The starting materials used in the last-mentioned process may be obtained by the acylation of the corresponding amino compound with an acylating agent derived from the acid of the formula R2COOH, wherein R2 has the meaning stated above. A suitable acylating agent is, for 10 example, an acyl halide or acid anhydride, or the acid itself in the presence of a condensing agent, for exaniple a carbodiimide. According to a further feature of the invention we provide a process for the manufacture of those of the al- 15 kanolamine derivatives of the invention wherein R4 stands for an acyl radical which comprises the interaction of an acid-addition salt of the corresponding alkanolamine derivative wherein R4 stands for hydrogen with an acylating agent derived from an acid of the formula R40H, 20 wherein R4 stands for an acyl radical. As a suitable acylating agent there may be mentioned, for example, an acyl halide or acid anhydride, for example acetic anhydride, acetyl chloride or benzoyl chloride. The acylation may be carried out in a diluent or 25 solvent, which, in the case where an acid anhydride is used as acylating agent, may conveniently be the acid from which the anhydride is derived. As stated above, the alkanolamine derivatives of the present invention are of value in the treatment or prophy- 30 laxis of heart diseases. Furthermore, some of the alkanolamine derivatives of the invention possess selective padrener-ic blocking activity. Compounds exhibiting this selective action show a greater degree of specificity in blockin.- the cardiac p-receptors than the P-receptors in 35 peripheral blood vessels and bronchial muscle. Thus, a dose may be selected for such a compound at which the compound blocks the cardiac inotropic and chronotropic actions of a catecholamine [for example isoprenaline, that is, I - (3,4-dihydroxyphenyl) - 2 - isopropylamino- 40 ethanol] but does not block the relaxation of tracheal smooth muscle produced by isoprenaline or the - peripheral vasodilator action of isoprenaline. Because of this selective action, one of these compounds may advantageously be used together with a sympathomimetic bronchodilator, 45 for example isoprenaline, orciprenaline, adrenaline or ephedrine, in the treatment of asthma and other obstructive airways diseases, inasmuch as the selective compound will substantially inhibit the unwanted stimulatory effects of the bronchodilator on the heart but will not hinder the 50 desirable therapeutic effect of the bronchodilator. According to a further feature of the invention, therefore, we provide pharmaceutical compositions comprising as active ingredient one or more alkanolamine derivatives of the invention, or acid-addition salts thereof, in 55 association with a pharmaceutically-acceptable diluent or carrier therefor. As stiitable compositions there may be mentioned, for example, tablets, capsules, aqueous or oily solutions or suspensions, emulsions, injectable aqueous or oily solti- 60 tions or suspensions, dispersible powders and aerosol formulations. The pharmaceutical compositions of the invention may contain, in addition to the alkanolamine derivatives of the invention, one or more additional drugs selected from 65 sedatives, for eximple phenobarbitone, meprobamate and chlorpromazine; vasodilators, for example glyceryl trinitrate, pentaerythritol tetranitrate and isosorbide dinitrate; diuretics, for example chlorothiazide; hypotensive agents, for example reserpine, bethanidine and guanethi- 70 dine; myocardial depressants, for example quinidine; and agents used in the treatment of Parkinsonism, for example benzhexol. Those of the pharmaceutical compositions of the invention which contain an alkanolamine derivative which possesses selective 6-adrenergic blocking 75 6 properties as stated above may additionally contain a sympathomimetic bronchodilator, for example isoprenaline, orciprenaline, adrenaline or ephedrine. It is expected that the preferred compounds would be given to man at an oral dose of between 20 mg. and 400 mg. daily, at doses spaced at 4-6 hourly intervals, or at an intravenous dose of between I mg. and 20 mg. daily. Preferred oral dosage forms are tablets or capsules containing 10 mg. or 40 mg. of active ingredient. Preferred intravenous dosage forms are sterile aqueous solutions of non-toxic acid addition salts of the alkanolamine derivatives, containing between 0.05% and 1% w./v. of active ingredient, and more particularly containing 0.1% w./v. of active ingredient. The invention is illustrated but not limited by the following examples in which the parts are by weight: EXAMPLE I A mixture of 0.5 part of propionyl chloride in 25 parts of ether is added to a stirred solution of 1.55 parts of 1(4 - aminophenoxy) - 3 - (N-benzyl-N-isopropylamino)2- propanol in 50 parts of ether which is maintained at 15' C. The mixture is stirred for 2 hours and is then evaporated to dryness under reduced pressure. The residue is dissolved in 50 parts of ethanol, 0.4 part of a 5% palladium-on-charcoal catalyst is added, and the mixture is shaken with hydrogen at a pressure of 100 atmospheres and at ambient temperature until uptake of hydrogen ceases. The mixture is filtered and the filtrate is evaporated to dryness under reduced pressure. The residue is dissolved in 50 parts of aqueous 2 N-hydrochloric acid, treated with carbon and filtered. The filtrate is poured into 50 parts of aqueous 2 N-sodium hydroxide solution and the mixture is filtered. The solid residue is washed with water, dried and crystallised from ethyl acetate. There is thus obtained 3 - isopropylamino - I - (4-propionamidophenoxy)-2- propanol, M.P. 135-137' C. EXAMPLE 2 A mixture of 1.5 parts of I - (5 - acetamido-2-n-butylphenoxy) - 2,3 - epoxypropane and 10 parts of isopropylamine is heated under reflux for 2 hours. The mixture is evaporated to dryness under reduced pressure, the residue is shaken with 25 parts of aqueous N-acetic acid and the mixture is extracted twice with 25 parts of ether each time. The aqueous phase is separated and added to 25 parts of aqueous 5 N-sodium hydroxide solution. The mixture is extracted three times with 25 parts of ether each time and the combined ethereal extracts are dried over anhydrous magnesium sulphate. The mixture is filtered and the filtrate is evaporated to dryness under reduced presstire. The residue is crystallised from a mixture of 15 parts of ethyl acetate and 0.5 part of water. There is thus obtained I - (5 - acetamido - 2-n-butylphenoxy)-3- isopropylamino - 2 - propanol hemihydrate, M.P. 131132'C. The I - (5 - acetamido - 2-n-butylphenoxy)-2,3-epoxypropane used as starting material may be obtained as follows: A mixture of I part of 5 - acetamido - 2 - n-butylphenol, 0.2 part of sodium hydroxide, 0.7 part of epichlorohydrin, 2 parts of water and 20 parts of methanol is heated under reflux for 2 hours. The mixture is evaporated to dryness under reduced pressure. The residue consists of 1-(5-acetamido-2-n-butylphenoxy )-2,3-epoxypropane. EXAMPLE 3 A solution of 0.4 part of acetyl chloride in 25 parts of ether is added to a stirred solution of 1.6 parts of 1-(4amino - 3 - methylphenoxy) - 3- (N-benzyl-N-isopropylamino-2- propanol in 50 paris of ether which is maintained at 15' C. The mixture is stirred for 2 hours and the ethereal layer is then decanted off. The residue is dissolved in 50 parts of ethanol, 0.3 part of a 5% palladiumon-charcoal catalyst is added, and the mixture is shaken
[4]7 with hydrogen at atmospheric pressure and ambient temperature until the uptake of hydrogen ceases. The mixture is filtered and the filtrate is evaporated to dryness under reduced pressure. The residue is dissolved in 10 parts of water and the solution is treated with carbon and filtered. The filtrate is poured into 25 parts of aqueous Nsodium hydroxide solution and the mixture is stirred with 50 parts of ether. The mixture is filtered and the solid residue is washed with ether and crystallised from etbyl methyl ketone. Thore is thus obtained 1-(4-acetamido - 3 - methylphenoxy) - 3-isopropylamino2-propanol, M.P. 165' C. The I - (4 - amino - 3-methylphenoxy)-3-(N-benzyl-N isopropylamino) - 2 - propanol used as starting material may be obtained as follows: 15.6 parts of epichlorohydrin are added to a SOILItion of 4.5 parts of 3 - methyl - 4 - nitrophenol and 1.32 parts of sodium hydroxide in 50 parts of water which is maintained at 15' C. The mixti-ire is stirred at ambient temperature for 16 hours and is then extracted with 50 parts of chloroform. The chloroform extract is dried over anhydrous magnesium sulphate, the mixture is filtered and the filtrate is evaporated to dryness under reduced pressure. The residue consists of I - (3 - methyl - 4-nitrophenoxy)-2,3-epoxypropane. A mixture of 6 parts of the above compound and 4.5 parts of N - benzyl - N - isopropylamine is heated at 100' C. for 2 hours. The mixture is then extracted 4 times with petroleum ether (B.P. 80-100' C.) and the extracts are combined and evaporated to dryness under reduced pressure. There is thus obtained I - (3 - methyl - 4- nitrophenoxy)-3-(N-benzyl-N-isopropylaniino)-2-propanol. A solution of 5.6 parts of the above compound in 50 parts of ethanol is added dropwise to a rapidly stii@red mixture of 16 parts of iron powder, 63 parts of ethanol and 0.26 part of concentrated hydrochloric acid whicb. is heated under reflux. The mixture is stirred and heated under reflux for 1 hour, 0.26 part of concentrated hydrochloric acid is added, and the mixture is stirred and heated under reflux for a ftirther 2 hours. 4 parts of aqueous 10 N-sodium hydroxide solution are then added and the hot mixture is filtered. The filtrate is evaporated to dryness under reduced pressure and the residue is stirred with 50 parts of aqueous N-bydrocbloric acid and 50 parts of ether. The aqueous acidic phase is separated, treated with carbon, filtered and the filtrate is added to 50 parts of aqueous 2 N-sodium bydroxide solution. The mixture is extracted twice with 50 parts of ether each time and the ethereal extracts are combined and dried with anhydrous magnesium sulphate. The mixture is filtered and the filtrate is evaporated to dryness under reduced pressure. The residue consists of 1 - (4 - amino - 3- methylphenoxy)3-(N-benzyl-N-isopropylamino)-2-propanol. EXAMPLE 4 The process described in Example I is repeated except that 0.9 part of phenoxyacetyl chloride is used in place of the 0.5 part of propionyl chloride. The hydrogenation mixture is filtered and the filtrate is evaporated to dryness under reduced pressure. The residue is crystallised from isopropanol and there is thus obtained 3isopropylamino - 1 - (4 - phenoxyacetamidophenoxy)-2propanol hydrochloi-ide, M.P. 168-170' C. EXAMPLE 5 A mixture of 2 parts of I - (4 - acetamidophenoxy)- 3isopropylamino - 2 - propanol hydrochloride and 20 parts of acetyl chloride is heated under reflux for 3 hours. The mixture is cooled and filtered and the solid residue is washed with acetone. There is thus obtained 1-(4-acetamidophenoxymethyl) - 2 - is opropylaminoethyl acetate hydrochloride, M.P. 134-1361 C. with decomposition. EXAMPLE 6 A mixttire of 0.35 part of acetyl chloride in 25 parts of ether is added to a stirred mixture of 0.75 part of 1-(2- 3)562)297 8 aminophenoxy)-3-(N-benzyl-N-isopropylamino) - 2-propanol in 50 parts of ether maintained at 15' C. The mixture is stirred for I hour and evaporated to dryness under reduced presslire. The residue is dissolved in 50 parts of ethanol, 0.5 part of a 5% palladium-on-charcoal catalyst is added, and the mixture is shaken with hydrogen at ambient temperature and atmospheric pressure until the uptake of hydro.-en ceases. The mixture is filtered and the filtrate is evaporated to dryness under reduced pres10 sure. The residue is dissolved in 10 parts of water, and the so]Lttion is basified with aqueous 11 N-sodium hydroxide solution and extracted with 50 parts of ether. The ethereal extract is dried over anhydrous magnesium sulphate and filtered, and the filtrate is evaporated to dryness 15 under reduced pressure. The residue is crystallised froiii ethyt methyl ketone and there is thus obtained 1-(2acetamidophenoxy)-3- isopropylamino - 2 - propanol, M.P. 98-100, C. EXAMPLE 7 20 A solution of 0.8 part of chloroacetyl chloride in 25 parts of ether is added to a stirred solution of 1.5 parts of 1-(4-aminophenoxy)-3-(Nbenzyl - N - isopropylamino)2-propanol in 50 parts of ether which is maintained at 25 15' C. The mixture is stirred for 2 hours and then evaporated to dryness under reduced pressure. The residue is dissolved in 50 parts of ethanol and 0.5 part of a 5% palladium-on-charcoal catalyst is added. The mixture is shaken with hydrogen at atmospheric pressure and ambi30 ent temperature until uptake of hydrogen ceases. The mix@ ttire is filtered and the filtrate is evaporated to dryness under reduced pressure. The residue is crystallised from isopropanol and there is thus obtained 1-(4- chloroacetainidophenoxy) - 3 - isopropylaminc@-2-propanol, M.P. 146- 48' C. 35 EXAMPLE 8 A mixture of 3.4 parts of 1-(4-cyclohexanecarbonamidophenoxy) - 3-(Nbenzyl-N-isopropylamino)-2-propanol, 100 parts of ethanol and 1.5 parts of a 5% palladi40 um-on-charcoal catalyst is shaken with hydro,-en at ambient temperature and atmospheric pressure for 1.6 hours when theoretical uptake of hydrogen is complete. The mixture is filtered and the filtrate is evaporated to dryness. The residue is crystallised three times from ethyl 45 acetate and there is thus obtained 1-(4-cyclohex anecarbonamidophenoxy) - 3 - isopropylamino-2-propanol, M.P, 159-161' C. The I - (4 - cyclohexanecarbonamidophenoxy) - 3 - (Nbenzyl - N - isopropylamino) -2-propanol used as starting 50 material may be obtained as follows: A solution of 1.27 parts of cyclohexanecarboxylic acid and 3.14 parts of 1-(4- aminophenoxy) - 3 - (N-benzyl-Nisopropylamino)-2-propanol in 40 parts of ethyl acetate is stirred at O' C. and a solution of 2.3 parts of N,N'-di55 cyclohexylcarbodi-imide in 10 parts of ethyl acetate is rapidly added. The mixture is stirred for 2 hours at ambient temperature and is then filtered. The filtrate is extracted three times with 80 parts of aqueous 2 N-hydrochloric acid each time, and the combined acidic extracts 60 are basified with aqueous potassium hydroxide solution. The basic mixture is extracted with ethyl acetate and the extract is dried and evaporated to dryness. There is thus obtained as residue I - (4-cyclohexan ecarbonamidophenoxy)-3-(Nbenzyl-N-isopropylamino)-2-propanol. 65 EXAMPLE 9 The process described in the first part of Example 8 is repeated except that the appropriate starting material is used in place of 1-(4- cyclohexanecarbonamidophenoxy)- 70 3-(N-benzyl-N-isopropylamino) - 2 - propanol. There are thus obtained the products described in the followi'ng table. RINTI-E -0 01-120HOI-ICII2NHCH(CI13)2 75
[5]8,562)297 9 M.P. Reciystallisatioll RO ('C.) solvent liydroxyacetyl ----------------------------- 125-128 Ethyl C tate. a e 2-furoyl ------------------------------------- 138-141 - Benzene. Cyclopropanecarbonyl ---------------------- 159-160 Ethyl acetate. The starting materials used in the above process may be obtained by the procedure described in the second part of Example 8 except that the appropriate carboxylic acid is used in place of cyclohexanecarboxylic acid. EXAMPLE 10 A mixture of 4.75 parts of 1-[4-(p-acetamidobenz am ido)phenoxyl-3-(N-benzyl-Nisopropylamino) - 2 - propanol hydrochloride, 0.27 part of a 5% palladium-oncharcoal catalyst and 50 parts of ethanol is shaken with hydrogen at atmospheric pressure and at ambient temperature until uptake of hydrogen ceases. The mixture is filtered and the filtrate is evaporated to dryness under reduced pressure. The residue is dissolved in 25 parts of water, and the solution is basified with aqueous 11 Nsodium hydroxide solution and stirred with 25 parts of ethyl acetate. The mixture is filtered and the solid residue is crystallised from methanol. There is thus obtained 1-[4(pacetamidobenzamido)phenoxyl - 3 - isopropylamino2-propanol, M.P. 210-21Z' C. The 1-[4-(p-acetamidobenzamido)phenoxyl3-(N-benzyl-N-isopropylamino)-2- propanol hydrochloride used as starting material may be obtained as follows: A solution of 3.7 parts of p-nitrobenzoyl chloride in 50 parts of ether and 30 parts of ethyl acetate is added to a stirred mixture of 6 parts of 1-(4-aminophenoxy)-3-(Nbenzyl - N - isopropylamino)-2-propanol in 200 parts of ether wbich is maintained at 15' C. The mixture is stirred for 2 hours and filtered and the solid residue is crystallised from methanol. There is thus obtained 1-[4-(p-nitrobenzamido)phenoxy] - 3 - (N-benzyl-Nisopropylamino)2-propanol hydrochloride, M.P. 230-2321 C. A solution of 5 parts of the above compound in 60 parts of ethanol and 10 parts of water is added dropwise to a stirred mixture of 375 parts of ethanol, 93.6 parts of iron powder and 1.56 parts of aqueous 11 N-hydrochloric acid which is heated under reflux. The mixture is stirred and heated under reflux for 3 hours, 12.6 parts of aqueous 11 Nsodium hydroxide solution are then added, and the hot mixture is filtered. The filtrate is evaporated to dryness under reduced pressure and the residue is extracted with @50 parts of ethyl acetate. The ethyl acetate phase is separated, dried with anbydrous magnesium sulphate, filtered and the filtrate is evaporated to dryness under reduced pressure. There is thus obtained 1-[4 - (p - amino benzamido)phenoxyl-3-(Nbenzyl-Nisopropylamino) -2-propanol. A solution of I part of acetyl chloride in 25 parts of ether is added to a stirred solution of 4.32 parts of the above compound in 100 parts of benzene which is maintained at 15' C. The mixture is stirred for 2 hours and then filtered. The solid residue is washed with ether and there is thus obtained 1 - [4 - (p-acetam idobenzamido)phenoxyl - 3 - (N - benzyl - N - isopropylamino) - 2propanol hydrochloride. EXAMPLE I 1 A mixture of 2.8 parts of 1-(4 - m-nitrobenzamidoph enoxy)-2,3-epoxypropane and 20 parts of isopropylamine is heated under reflux for 3 bours. The mixture is evaporated to dryness under reduced pressure and the residue is shaken with 50 parts of aqueous Nhydrochloric acid md 50 parts of ethyl acetate. The acidic phase is spearated and poured into 10 parts, of aqueous 11 Nsodium hydroxide solution. The mixture is filtered and the solid residue is washed with water, dried and crystaIIised from isopropanol. There is thus obtained 3-isopropyla,mino - I - (4 - m -- nitrobenzamidophenoxy)2- propanol, M.P. 162-164' C. 10 The 1-(4 - m - nitrobenzamidophenoxy) - 2,3-epoxypropane used as startinmaterial may be obtained as I(iiows: 2.4 parts of epichlorohydrin are added to a solution of 2.5 parts of 4-mnitrobenzamidophenol and 0.4 part of sodium hydroxide in 50 parts of water which is maintained at 15' C. The mixture is stirred at ambient temperature for 5 hours and is then extracted twice with 50 parts of chloroform each time. The chloroform extracts are combined, dried with anhydrous magnesium sulphate, and evaporated to dryness under reduced pressure. The residue consists of I - (4 - m - nitrobenzamidophenoxy)2,3-epoxypropane. 15 EYAMPLE 12 A solution of 1.6 parts of p-toltioyl chloride in 25 parts of ether is added to a stirred solution of 1.5 parts of 1-(4-aminophenoxy) - 3 - (N - benzyl-N-isopropylamino) - 2 - propanol in 50 parts of ether wbich is main20 tained at 15' C. The mixture is stirred for 2 bours and is then evaporated to dryness under reduced pressure. The residue is dissolved in 50 parts of ethanol, 0.5 part of a 5% palladium-on-charcoal catalyst is added, and the mixture is shaken with hydrogen at atmospheric pres25 sure and ambient temperature until uptake of hydrogen ceases. The mixture is filtered and the filtrate is evaporated to dryness under reduced pressure. The residue is shaken with 25 parts of water, 5 parts of aqueous 2 N-hydrochloric acid and 25 parts of ethyl acetate. The mixture 30 is filtered, and the acidic phase is separated and added to 25 parts of aqueous 2 Nsodium hydroxide solution. The mixture is filtered and the solid residue is washed with water, dried and crystallised from isopropanol. There is thus obtained 3- isopropylamino - I - (4-p-toluamido35 phenoxy)-2-propanol, M.P. 176' C. EXAMPLE 13 0.4 part of a 5% palladium-on-charcoal catalyst is added to a solution of 1.1 parts of 1-(4 - for-mamido40 phenoxy) - 3 - N - benzyl - N-isopropylamino-2-propanol in 30 parts of ethanol, and the mixture is shaken with hydrogen at atmospheric pressure and ambient temperature until uptake of hydrogen is complete. The mixture is filtered and the filtrate is evaporated to dryness. The 45 residue is crystallised from etha-nol and there is thus obtained l@(4- formamidophenoxy) - 3 - isopropylamino2-propanol dihydrate, M.P. 189-192' C. The I - (4 - formamidophenoxy) - 3 - N-benzyl-Nisopropylamino-2-propanol used as starting material in 5o the above process may be prepared as follows: 21.6 parts of acetic anhydride are added dropwise during 1 hour to a stirred solution of 4 parts of 1-(4-aminophenoxy)-3-N-benzy l-N-isopropylamino - 2 - propanol in 57.3 parts of 98% formic acid which is maintained at 55 5-10' C. The mixture is stirred for 6 hours at ambient temperature, 20 parts of icewater are added, and aqueous sodium hydroxide solution is then added until the mixture is alkaline. The mixture is extracted twice with 300 parts of chloroform each time and the combined extracts 60 are dried and evaporated to dryness. There is thus obtained 1-(4- formamidophenoxy) - 3 - N - benzyl - Nisopropylamin o-2-propanol. EXAMP.LE 14 65 A solution of 2.57 parts of N,N' - dicyclohexylcarbodiimide in 20 parts of ethyl acetate is added dropwise during 2 minutes to a stirred mixture of 3.15 parts of acrylic acid, 2.0 parts of I (4 - aminophenoxy) - 3 isopropylaminopropan - 2 ol and 30 parts of ethyl 70 acetate which is maintained between 0 and 5' C. The mixture is stirred at 0-5' C. for a further 30 minutes, 65 parts of aqueous 2 N-hydrochloric acid are added and the mixture is vigorously shaken and then filtered through a filteraid. The aqueous phase is separated, basified with 75 concentrated aqueous sodium hydroxide solution with
[6]cooling and stirring, 'and then extracted twice with 50 parts of ethyl acetate each time. The extracts are washed with 20 parts of water, dried, and evaporated to dryness at ambient temperature. The residue is crystallised from ethyl acetate and there is thiis obtained 1-(4-acrylamidophenoxy) - 3 - isopropylaminopropan-2-ol, M.P. 127-132' C. containing one qiiarter of -,t molecule of water of crystallisation. EXAMPLE 15 A mixture of 2.07 parts of 1-(4-acetamidopheiioxy)2 ,3-epoxypropane, 10 parts of ethanol and 1.5 parts of cyclopropylamine is heated in a sealed vessel at 100' C. for 10 hours. The mixture is evaporated to dryness under reduced pressure and the residue is crystallised from 10 parts of ethyl acetate. There is thus obtained I - (4acetamidophenoxy) - 3 - cyclopropylamino-2-propanol, M.P. 114-116' C. EXAMPLE 16 A mixture of I part of 1-(4-acetamidophenoxy)-2,3epoxypropane, 25 parts of etbanol and 25 parts of a 33% solution of methylamine in ethanol is heated under reflux for 4 hours. The mixture is evaporated to dryness under reduced pressure and the residue is crystallised from a mixture of 6 parts of ethyl acetate and 1 part of ethanol. There is thus obtained 1-(4-acetamidophenoxy)3-methylamino-2-propanol, M.P. 122' C. EXAMPLE 17 A mixttire of 4.2 parts of 1-(3-acetamido-5-methylp henoxy)-3-chloro-2-pTopanol, 14 parts of isopropylamine and 20 parts of methanol is heated in a sealed tube at 110' C. for 12 hours. The mixttire is evaporated to dryness and the residue is shaken with a mixture of ethyl acetate and water. The organic layer is separated, dried and evaporated to dryness and the residue is purified by preparative thin-layer chromatography on silica gel plates using a 3% w./v. solution of triethylamine in eth,,inol as developing solvent. The purified product is crystallised from ethyl acetate and there is thus obtained 1-(3-acetamido - 5 - met hylphenoxy)-3-isopropylamino-2- propanol, M.P. 134.5-137' C. The 1 - (3 - acetamide-5-methylplienoxy)-3-chloro-2propanol used as startin.- material may be obtained as follows: A solution of 1.73 parts of 3-acetamide-5-nitrotoluene in 60 parts of ethanol is shaken with 0.85 part of a 5% palladium-on-charcoal catalyst in an atmosphere of hydrogen at atmospheric pressure for 1 hour. The mixture is filtered and the filtrate is evaporated to dryness. There is thus obtaided 3-ac etamide-5-aminotoluene as an oil. A solution of 0.68 part of sodium nitrite in 10 parts of water is added dropwise to a stirred solution of 1.45 parts of 3-acetamido-5-aminotoluene in 45 parts of water containing 3.3 parts of sulphuric acid which is maintained between 5 and 10' C. The resulting suspension is added during 10 minutes to 50 parts of boiling water, and the mixture is cooled and extracted three times with 100 parts of ethyl acetate each time. The extract is dried and evaporated to dryness and the residue is piirified by preparative thin-layer chromato@raphy on silica -el plates using a mixture of 3 parts of triethylamine, 20 parts of ethanol and 100 parts of ethyl acetate as developin,- solvent. The -major band is eluted with methanol, the methanol solution is evaporated to dryness and the residue is dissolved in ethyl acetate. The solution is extracted with 10% aqueous potassium hydroxide solution and the extract is acidified and then extracted witji ethyl acetate. The extract is dried and evaporated to dryness and there is thus obtained as residue 3-acetamido-5-methylphenol. A mixttire of 2 parts of 3-acetamido-5-methylphenol 15 parts of epichlorohydrin, 0.05 part of piperidine and 10 parts of isopropanol is heated at 95-100' C. for 6 holirs. The mixture is evaporated to dryness under re3)562,297 12 duced pressure and the residue consists of 1-(3-ace tamido-5-methylphenoxy-3- isopropylamino-2-propanol. EXAMPLE 18 5 A solution of 6 parts of 1-chloro-3-(4-propionamido phenoxy)-propan-2-ol and 11.5 parts of t-butylamine in 15 parts of niethanol is heated in a scaled tube for 12 10 hotirs at 110' C. The solution is evaporated to dryn-.ss, the residue is dissolved in 80 parts of ethyl acetate and the mixture is extracted twice with 50 parts of aqueous 2 N-hydrochloric acid each time. The acidic layer is washed with 30 parts of ethyl acetate and basified and the 15 mixture is extracted successively with 100 parts and 50 parts of ethyl acetate. The combined organic extracts are washed with 20 parts of water, dried and evaporated to dryness. The residue is crystallised from a mixture of ethyl acetate and hexane, and there is thus obtained 1-(4- 20 propionamidophenoxy)-3-t-butylaminopropan-2-ol, M.P. 99-101.5' C. The 1- chloro-3-(4-propionamidophenoxy)propan-2-ol used as starting material may be obtained as follows: A mixture of 3.95 parts of 4-propionamidophenol, 30 25 parts of of epichlorhydrin and 0.05 part of piperidille is heated for six hours at 95- 100' C. The excess of epichlorhydrin is removed by evaporation under reduced pressiire and there is thus obtained 1-chloro-3-(4- propionamidophenoxy) propan-2-ol as an oil. 30 What we
