WO1998011064A1

WO1998011064A1 - Stereospecific preparation of chiral 1-aryl- and 1-heteroaryl-2-substituted ethyl-2-amines

Info

Publication number: WO1998011064A1
Application number: PCT/US1997/015729
Authority: WO
Inventors: Luc Grondard; Jean-Paul Casimir; Patrick Leon; Michael K. O'brien; Matthew R. Powers; Daniel Robin
Original assignee: Rhone-Poulenc Rorer Pharmaceuticals Inc.
Priority date: 1996-09-12
Filing date: 1997-09-10
Publication date: 1998-03-19
Also published as: AU4256297A; UA54451C2; US6127550A; HK1022296A1; JP2001501922A; KR20000036007A; BR9711466A; OA10991A; CN1388119A; AU732332B2; BG103259A; EA001364B1; AP937A; KR100317871B1; SK26999A3; CN1230176A; US6433172B1; EP0942900A4; CA2265886A1; HUP0000219A3

Abstract

This invention is directed to methods for stereospecifically preparing [(1-optionally substituted aryl)- or (1-optionally substituted heteroaryl)]-2-substituted ethyl-2-amines, having chirality at the 2-position, and to intermediates to the substituted ethyl-2-amines.

Description

STEREOSPECIFIC PREPARATION OF CHIRAL l-ARYL- AND l-HETEROARYL-2-SUBSTITUTED ETHYL-2-AMINES

FIELD OF THE INVENTION This invention is directed to methods for stereospecifically preparing [(1 -optionally substituted aryl)- or ( 1-optionally substituted heteroaryl)]-2-substituted ethyl-2-amines, having chirality at the 2-position. The invention is directed also to intermediates to the substituted ethyl-2-amines.

The substituted ethyl-2-amines, and intermediate compounds thereto, are useful as intermediates in the synthesis of cardiovascular agents, including antihypertensive agents, anti- ischemic agents, cardioprotective agents which ameliorate ischemic injury or myocardial infarcl size consequent to myocardial ischemia, and antilipolytic agents which reduce plasma lipid levels, serum triglyceride levels, and plasma cholesterol levels.

For example, the substituted ethyl-2-amines are useful as intermediates in the preparation of antihypertensive and anti-ische ic heterocyclyl adenosine derivatives and analogues as disclosed in U.S. Patent 5,364.862. They are useful also in the preparation of N₉-cyclopentyl-substituted adenine derivatives reported to be adenosine receptor ligands, and useful in cardiovascular conditions such as hypertension, thrombosis and atherosclerosis, and also in central nervous system conditions comprising psychotic conditions such as schizophrenia, and convulsive disorders such as epilepsy, as disclosed in U.S. Patent 4.954,504. They are useful also in the preparation of N-6 and 5'-N substituted carboxamidoadenosine derivatives which have beneficial cardiovascular and antihypertensive activity as reported in U.S. Patent 5,310,731.

REPORTED DEVELOPMENTS Stereospecific preparation of chiral optionally substituted heteroaryl-2-substituted ethyl 2- amines by reaction of heteroaryl anions with 2-substituted ethylene oxides, and subsequent stereospecific conversion of the resulting chiral ethyl alcohol to the amine has been reported by Spada et al., in U.S. Patent 5,364,862.

Facilitation of acidolytic cleavage reactions, for example the removal of various protecting groups, in the presence of electrophilic scavengers has been reported. Deprotection of N^G- mesitylene-2-sulfonylarginine is reported by Yajima et al.. Chem. Pharm. Bull. 26 (12) 3752-3757 (1978). Removal of the protecting group of O-benzyl serine, fhreonine, and tyrosine, and deprotection of N' -benzyloxycarbonyllysine is reported by Kiso et al., Chem. Pharm. Bull. 28 (2)

673-676 (1980). Deprotection procedures for the p-toluenesulfonyl and p-methoxybenzenesulfonyl groups from the N^im-function of histidine is reported by and Kitagawa et al., Chem. Pharm. Bull. 28 (3) 926-931 (1980). SUMMARY OF THE INVENTION The present invention is directed to methods for stereospecifically preparing [(1 -optionally substituted aryl)- or (1-optionally substituted heteroaryI)l-2-substituted ethyl-2-amines, having chirality at the 2-posiϋon. comprising reacting a 2-amino-2-substituted ethyl alcohol, having chirality at the 2-position, with an [(optionally substituted aryl)- or (trihalomethyl) sult nylj- halide or anhydride in the presence of a base to form an [(N-arylsulfonyl)- or (N-trihalomethylsulfonyl)]-2- substituted aziridine having chirality at the 2-position.

DETAILED DESCRIPTION

As used above, and throughout the description of this invention, the following terms, unless otherwise indicated, shall be understood to have the following meanings: "Aryl" means phenyl or naphthyl.

"Optionally substituted aryl" means an aryl group which be substituted with one or more aryl group substituents. Examples of aryl group substituents include alkyl, alkoxy, amino, aryl, heteroaryl, trihalomethyl, nitro, carboxy, carboalkoxy, carboxyalkyl, cyano, alkyla ino, halo, hydroxy, hydroxyalkyl, mercaptyl, alkyJmercaptyl, or carbamoyl. Preferred aryl group substituents include halo, hydroxy, alkyl, aryl, alkoxy, trihalomethyl, cyano, nitro, and alkyl mercaptyl.

"Heteroaryl" means about a 4 to about a 10 membered aromatic ring structure in which one or more of the atoms in the ring is an element other than carbon, e.g.. N, O or S. Examples of heteroaryl groups include pyridyl, pyridazinyl, pyrimidinyl, isoquinolinyl, quinolinyl, quinazolinyl, imidazolyl, pyrrolyl, furanyl, thienyl, thiazolyl, and benzothiazolyl. A preferred heteroaryl group is thienyl.

"Optionally substituted heteroaryl" means that the heteroaryl group may be substituted by one or more aryl group substituents. Examples of heteroaryl group substituents include alkoxy, alkylamino, aryl, carbalkoxy, carbamoyl, cyano, halo, heteroaryl. trihalomethyl, hydroxy, mercaptyl, alkylmercaptyl or nitro. Preferred heteroaryl group substituents include halo, hydroxy, alkyl, aryl, alkoxy. trihalomethyl. cyano. nitro. and alkylmercaptyl.

"Halogen" ("halo", "halide") means chlorine (chloro, chloride), fluorine (fluoro, fluoride), bromine (bromo, bromide) or iodine (iodo, iodide).

".Alky!" means a saturated aliphatic hydrocarbon group which may be straight or branched and having about 1 to about 20 carbon atoms in the chain. Preferred alkyl groups may be straight or branched and have about 1 to about 10 carbon atoms in the chain. Lower alkyl means an alkyl group which may be straight or branched having about 1 to about 6 carbon atoms, such as methyl, ethyl, propyl or tert-butyl. Branched means that a lower alkyl group is attached to a linear alkyl chain. "Aralkyl" means an alkyl group substituted by an aryl group. "Optionally substituted aralkyl" means that the aryl group of the aralkyl group may be substituted with one or more aryl group substituents.

"Heteroaralkyl" means an alkyl group substituted by a heteroaryl group. "Optionally substituted heteroaralkyl" means that the heteroaryl group or the heteroaralkyl group may be substituted with one or more aryl group substituents.

"Electrophilic scavenger" means an agent that can have a promoting effect on acidolytic cleavage reactions, for example, as described by Yaji a et al.. Chem. Pharm. Bull. 26 (12) 3752- 3757 ( 1978), Kiso et al., Chem. Pharm. Bull. 28 (2) 673-676 (1980), and Kitagawa et al.. Chem. Pharm. BulL 2S (3) 926-931 ( 1980).

An embodiment according to the invention is directed to a reaction of a 2-amino-2- substituted ethyl alcohol with a sulfonyl halide or anhydride, preferably in the presence of an aprotic organic solvent. Aprotic organic solvents which are suitable for the reaction include aprotic organic ethers, aromatic hydrocarbons, heteroaro atic hydrocarbons, aliphatic hydrocarbons, and aprotic organic amides. More particularly, examples of suitable aprotic organic solvents include diethyl ether, tert-butyl methyl ether, isopropyl methyl ether, diisopropyl ether, tetrahydrofuran, tetrahydropyran, and dioxan. In a special embodiment of methods according to the invention, the preferred aprotic organic solvent is tert-butyl methyl ether.

The reaction with the sulfonyl halide or anhydride takes place preferably at a temperature range from about 25°C to about 90°C; more preferably from about 25°C to about 40°C.

Suitable sulfonyl halides and anhydrides include phenyl-, tol-4-yl-, 2,4,6-trimethyIphenyl-, 2,4-dimethylphenyl-, 4-methoxyphenyl-, 4-nitrophenyl-, 4-bromophenyl-, naphth-1-yl-, naphth-2- yl-, and trifluoromethyl- sulfonyl chloride and anhydride. In a special embodiment of methods according to the invention, a preferred sulfonyl chloride is p-toluenesulfonyl chloride (i.e., tol-4-yl sulfonyl chloride).

According to the invention, the reaction of the 2-amino-2 -substituted ethyl alcohol with the sulfonyl halide or anhydride takes place in the presence of a base. Bases which are suitable for the reaction include aqueous alkali metal hydroxides, aqueous alkali metal carbonates, and aprotic organic amines. More particularly, examples of suitable alkali metal hydroxides include sodium hydroxide, potassium hydroxide, and lithium hydroxide; examples of suitable alkali metal carbonates include potassium carbonate, sodium carbonate, and cesium carbonate; and examples of suitable aprotic organic amines include triethylamine, diisopropyl ethyl amine, N-methylmorpholine, and pyridine. In a special embodiment of methods according to the invention, a preferred base is aqueous sodium hydroxide. Another embodiment according to the invention is directed to the reaction of the

[(N-arylsulfonyl)- or (N-trihalomethylsulfonyl)]-2-substituted aziridine having chirality at the 2- position, which is formed from the reaction of the 2-amino-2-substiruted ethyl alcohol with the sulfonyl halide or anhydride, with an [(optionally substituted aryl)- or (optionally substituted heteroaryl)] lithium compound to form the lithium salt of an [(N-optionally substituted aryl)- or (N- trihalomethyl)sulfonyl]-l- [(optionally substituted aryl)- or (optionally substituted heteroaryl)]-2- substituted alkyl-2-amine having chirality at the 2-position. In a special embodiment of the invention, the lithium salt formed in the reaction is isolated as a solid. Organolithium compounds may exist as tetramers, hexamers, and higher aggregates in hydrocarbon and ether solvents, as described, for example, by Carey, F.A., and Sundberg, Richard J., Advanced Organic Chemistry, Plenum Press, New York (2d ed. 1984), and Fraenkel et al., J. Am. Chem. Soc. 102, 3345 (1980). Formation by methods according to the invention of such aggregates of the lithium salts, and the aggregates so-formed are contemplated by and included in the invention. The reaction to form lithium salt takes place preferably in an aprotic organic solvent.

Aprotic organic solvents which are suitable for the reaction include aprotic organic ethers, aliphatic hydrocarbons, and aromatic hydrocarbons. In a special embodiment of methods according to the invention, a preferred aprotic organic solvent is an aprotic organic ether and, more particularly, tert- butyl methyl ether. The formation of the lithium salt takes place preferably at about -80°C to about 50°C; more preferably at about -40°C to about 50°C.

Yet another embodiment according to the invention is directed to the treatment of the lithium salt of an [(N-optionally substituted aryl)- or (N-trihalomethyl)sulfonylj-l- [(optionally substituted aryl)- or (optionally substituted heteroaryl)]-2-substituted alkyl-2-amine having chirality at the 2- position with one or more strong acids in the presence of an electrophilic scavenger. This treatment takes place preferably at a temperature range of about 45°C to about reflux.

Strong acids which are suitable for the treatment include methanesulfonic acid, trifluoroacetic acid, trifluoromethanesulfonic acid, trichloromefhane sulfonic acid, trichloroacetic acid, sulfuric acid, hydrochloric acid, hydrobromic acid, and phosphoric acid. In a special embodiment of the invention, the treatment takes place preferably in a mixture of strong acids; more preferably in a mixture of methanesulfonic acid and trifluoroacetic acid.

Electrophilic scavengers which are suitable for the treatment include anisole, thioanisole, diphenyldisulfide, phenylbenzylsulfide, trimethoxybenzenc, m-cresol, and 1,2-ethanediol. In a special embodiment according to the invention, a preferred electrophilic scavenger is thioanisole. A preferred embodiment according to the invention is a method for preparing a compound of Formula I,

Formula I wherein * indicates a chiral carbon atom,

R, is optionally substituted aryl, or optionally substituted heteroaryl; and R, is optionally substituted alkyl, optionally substituted aryl, optionally substituted aralkyl, optionally substituted heteroaryl, or optionally substituted heteroaralkyl, comprising reacting a compound of Formula II

Formula II with a compound of Formula III

R,-S0₂-R' Formula III wherein

R' is halo or OSO₂R₂; and

R₂ is optionally substituted aryl, or trihalomethyl, in the presence of a base to form an aziridine compound of Formula IV.

S0₂R₂

Formula IV

A further preferred embodiment of the present invention is the method of preparing a compound of Formula I wherein R, is optionally substituted heteroaryl; more preferably R, is 3- chlorothien-2-yl.

Another further preferred embodiment of the invention is the method for preparing the compound of Formula I wherein R₃ is alkyl; more preferably R, is ethyl.

Another preferred embodiment according to the invention is a method for preparing a compound of Formula I, comprising reacting the aziridine of Formula IV with a compound of formula Li-R, to form a lithium compound of Formula V,

Formula V or an aggregate thereof.

Another preferred embodiment according to the invention is a method for preparing a compound of Formula I, comprising treating the lithium compound of Formula V with a strong acid or mixture of strong acids in the presence of an electrophilic scavenger.

Preferred embodiments according to the invention are illustrated in Scheme I.

Rι-Li

Scheme I If it is necessary or desirable to prevent cross-reaction between chemically active substituents (for example, any aryl or heteroaryl group substituents) during the reactions or treatments of the methods according to the invention, the substituents may be protected by standard blocking groups which may be subsequently removed or retained, as required, by known methods to afford the desired product (see, for example, Green, Protective Groups in Organic Synthesis, Wiley, New York (1982)). Selective protection or deprotection also may be necessary or desirable to allow conversion or removal of existing substituents, or to allow subsequent reaction to afford the final desired product.

The present invention is directed also to intermediates to [(1 -optionally substituted aryl)- or (1-optionally substituted heteroaryl)]-2-substituted ethyl-2-amines.

A compound embodiment according to the invention is the [(N-arylsulfonyl)- or (N- trihalomethylsulfonyI)]-2-substituted aziridine having chirality at the 2-position, formed by the reaction of the of the 2-amino-2-substituted ethyl alcohol with the sulfonyl halide or anhydride according to the method of the invention. A preferred embodiment of said aziridine is the compound of Formula IV. A special embodiment of said aziridine includes 1-p-toluenesulfonyl- 2(R)-ethylaziridine. Another compound embodiment according invention is the lithium salt of an [(N-optionally substituted aryl)- or (N-trihalomethyl)sulfonyl]-l- Koptionally substituted aryl)- or (optionally substituted heteroaryl)]-2-substituted alkyl-2-amine having chirality at the 2-position formed by the reaction of the aziridine with an [(optionally substituted aryl)- or (optionally substituted heteroaryl)] lithium compound according to the method of the invention. A preferred embodiment of this lithium salt is the compound of Formula V. A special embodiment of the lithium salt includes is (R)- l-(3-chlorothien-2-yl)-2-butyltoluenesulfonamide lithium salt. The present invention is further explained, but is in no way limited, by the following examples.

EXAMPLE 1 Preparation of l-p-toluenesulfonyl-2(R)-ethylaziridine

R-(-)-2-amino-l-butanol (99.96 g.105 mL) and tert-butyl methyl ether (TBME) (277g, 366 mL) are combined under a nitrogen atmosphere. This mixture is stirred for several minutes and 10 N aqueous sodium hydroxide (449 mL) is added over a period of about 10 minutes. The reaction mixture is cooled to below 10°C and a solution of p-toluene sulfonyl chloride (TsCl) (464 g) in TBME (711 g) is added over a period of about 50 minutes, maintaining the temperature of the reaction mixture at or below 32°C. After the addition is complete, the mixture is stirred for about 30 minutes at 40°C, and water (900 mL) is added while cooling the mixture to 25°C. The layers are separated and the organic layer washed sequentially with water (150 g) and 25% aqueous sodium chloride solution (300 g). Toluene (450 g) is added to the organic layer, and the mixture distilled under reduced pressure, maintaining the temperature of the mixture at or below 45°C, until the water content of the mixture is below about 0.1%. The resulting solution is used, without further treatment, for the preparation described in Example 2.

EXAMPLE 2 Preparation of (R)-l -(3-chlorothien-2-yl)-2-butyltoluenesulfonamide lithium salt

Under a nitrogen atmosphere, a solution of 3-chlorothiophene (48.75 g) in TBME (291 g) is cooled to -10°C, and 2.5 M n-butyllithium in hexanes (151.3 mL) is added at such a rate that the reaction temperature is maintained between 0 and 5° C. After the addition is complete, the mixture is cooled to -5°C and l-p-toluenesulfonyl-2(R)-ethylaziridine (74.1 g, as a 56.9 % (w/w) solution in TBME) is added at such a rate to maintain the temperature of the reaction mixture below 9°C (during which time a solid precipitates). After about 5 minutes the mixture is cooled to 0° C and the precipitate is collected by vacuum filtration, washed with 0°C TBME (60 mL), and dried in vacuo at about 40°C, to give (R)-l-(3-chlorothien-2-yl)-2-butyltoluenesulfonamide lithium salt, m.p. 372°C (dec). MS (FAB), m z 350, 352 (100%), 'HNMR (200 Mhz, DMSO) 6 0.8 (t, 3H); 2.25 (s. 3H); 6.85 (d, 1H); 7.05 (d, 2H), 7.35 (d, 2H).

EXAMPLE 3

Preparation of (R)-l-(3-chlorothien-2-yl)-2-aminobutane

(R)-l-(3-chlorothien-2-yl)-2-butyltoluenesulfonamide lithium salt (120 g) is added in one portion to trifluoroacetic acid (470 g) in a vessel equipped with a condenser and mechanical stirrer. The temperature of the mixture rose from about 25°C to about 60°C. As the resulting solution is cooling, thioanisole (85.2 g) is added, followed by methanesulfonic acid (65.9 g). The reaction mixture is heated at 80°C for about six hours. The mixture is cooled to 18°C and toluene (600 mL) is added. 6M aqueous sodium hydroxide solution (820 mL) is then added portionwise, with stirring, maintaining the reaction temperature below 60°C. The layers are separated and the organic phase is washed with water until the pH of the wash is 9, then brine. The organic solution is cooled to 18°C and toluene (200 mL) is added followed concentrated hydrochloric acid (42 mL). The resulting slurry is distilled at about 47°C at 180 mm Hg to azeotropically remove water. After about 200 mL of toluene/water had been removed the mixture is cooled to 40°C, allowed to come to atmospheric pressure, then cooled to 15°C over a 1 hour period. The solids which precipitate are collected by vacuum filtration, washed with 60 mL of toluene and dried in vacuo to give (R)-l-(3-chlorothien-2- yl)-2-aminobutane as the hydrochloride salt, m.p. 137.6°C. MS (El), m/z 190, 192 (10%); 'HNMR (200 Mhz. DMSO) δ 0.9 (t. 3H); 1.6 (m. 2H); 7.05 (d, 1H); 7.6 (d, 2H), 8.35 (s, 2H).

Claims

WHAT IS CLAIMED IS:

1. A method for stereospecifically preparing a [(1 -optionally substituted aryl)- or (1 -optionally substituted heteroaryl)]-2-substituted ethyl-2-amine, having chirality at the 2-position, comprising reacting a 2-amino-2-substituted ethyl alcohol, having chirality at the 2-position, with an [(optionally substituted aryl)- or (trihalomethyl) sulfonyl]- halide or anhydride in the presence of a base to form an l(N-arylsulfonyl)- or (N-trihalomethylsulfonyl)]-2-substituted aziridine having chirality at the 2- position.

2. A method according to claim 1 further comprising reacting said aziridine with an

[(optionally substituted aryl)- or (optionally substituted heteroaryl)] lithium compound to form the lithium salt of an [(N-optionally substituted aryl)- or (N-trihalomethyl)sulfonyl]-l- [(optionally substituted aryl)- or (optionally substituted heteroaryl)]-2-substituted alkyI-2-amine having chirality at the 2-position.

3. A method according to claim 2 further comprising treating said lithium salt with one or more strong acids in die presence of an electrophilic scavenger.

4. A method according to claim 1 nd of formula

wherein

* indicates a chiral carbon atom,

R, is optionally substituted aryl, or optionally substituted heteroaryl; and

R₃ is optionally substituted alkyl, optionally substituted aryl, optionally substituted aralkyl, optionally substituted heteroaryl, or optionally substituted heteroaralkyl; comprising reacting a compound of formula

with a compound of formula R₂-SO₌-R' wherein R' is halo or OSO,R₂; and

R₂ is optionally substituted aryl, or trihalomethyl, in the presence of a base to form an aziridine compound of formula

5. A method according to claim 4 further comprising reacting said aziridine compound wiϋi a compound of formula Li-R,, to form a lithium compound of formula

, or an aggregate thereof.

6. A method according to claim 5 furtiier comprising treating said lithium compound with a strong acid or mixture of strong acids in the presence of an electrophilic scavenger.

7. A method according to claim 4 wherein said reacting occurs in an aprotic organic solvent.

8. A method according to claim 7 wherein said aprotic organic solvent is tert-butyl methyl ether.

9. A method according to claim 4 wherein R₂-S0₂-R' is p-toluenesulfonyl chloride.

10. A method according to claim 4 wherein said reacting occurs at about 25°C to about 90°C.

11. A method according to claim 4 wherein said reacting occurs at about 25°C to about 40°C.

12. A method according to claim 4 wherein said base is selected from the group consisting of an aqueous alkali metal hydroxide, an aqueous alkali metal carbonate, and an aprotic organic amine.

13. A method according to claim 4 wherein said base is aqueous sodium hydroxide.

14. A method according to claim 4 wherein R, is optionally substituted heteroaryl.

15. A method according to claim 14 wherein R, is 3-chlorothien-2-yl.

16. A mefiiod according to claim 4 wherein R₃ is alkyl.

17. A method according to claim 16 wherein R₃ is ethyl.

18. A method according to claim 5 wherein said reacting said aziridine compound occurs in a solvent selected from the group consisting of an aprotic organic ether, aliphatic hydrocarbon, and an aromatic hydrocarbon.

19. A method according to claim 18 wherein said reacting said aziridine compound occurs in tert-butyl methyl ether.

20. A method according to claim 5 further comprising isolating said lithium compound as a solid.

21. A method according to claim 5 wherein said reacting occurs at about -80°C to about 50°C.

22. A method according to claim 21 wherein said reacting occurs at about -40°C to about 50°C.

23. A method according to claim 6 wherein said mixture of strong acids comprises methanesulfonic acid and trifluoroacetic acid.

24. A method according to claim 6 wherein said electrophilic scavenger is thioanisole.

25. A method according to claim 6 wherein said treating occurs at about 45°C to about reflux.

26. The [(N-arylsulfonyl)- or (N-trihalomethylsulfonyl)]-2-substituied aziridine having chirality at die 2-position according to claim 1.

27. The aziridine compound according to claim 4 of formula

S0₂R₂

28. A compound according to claim 27 which is l-p-toluenesulfonyl-2(R)-ethylaziridine.

29. The litiiium salt of an [(N-optionally substituted aryl)- or (N-trihalomethyl)sulfonyl]-l- [(optionally substituted aryl)- or (optionally substituted heteroaryl)]-2-substituted alkyl-2-amine having chirality at the 2-position according to claim 2.

30. The lithium compound according to claim 5 of formula

^R2^S02\ ^ ⁱ N

Rι

¹³ , or an aggregate thereof.

31. A lithium compound according to claim 30 which is (R)-l-(3-chlorodιien-2-yl)-2- butyltoluenesulfonamide lithium salt.