Claims
- 1. A process for producing L-(-)-carnitine inner salt from D-(+)-carnitinamide which comprises:
- (a) hydrolyzing a salt of D-(+)-carnitinamide 1 of the general formula ##STR2## wherein X.sup.- is any monovalent counterion to obtain D-(+)-carnitine 2 ##STR3## (b) esterifying said D-(+)-carnitine 2 to an ester 3 of the general formula ##STR4## wherein R.sub.1 is (i) a straight or branched alkoxy group having 1-11 carbon atoms or (ii) an arylalkoxy or diarylalkoxy group wherein the aryl group is a monocyclic or bicyclic aryl group containing 5 to 12 carbon atoms and the alkyl group has 1-4 carbon atoms, and wherein said arylalkoxy or diarylalkoxy groups can be optionally substituted with a lower alkyl group having 1-4 carbon atoms, an alkoxy group having 1-4 carbon atoms, halogen, a nitro group or an amino group;
- (c) acylating said ester 3 to an acyl derivative 4 of the general formula ##STR5## wherein Y.sup.-, which is the same as or different than X.sup.-, is a counterion imparting solubility to 4 and OR is a leaving group wherein R is selected from an alkylsulfonyl having 1-12 carbon atoms, formyl and trifluoroacetyl,
- by reacting 3 with an acylating agent (1) of the formula RY wherein Y is a halogen or (2) an anhydride precursor for R, and R has the above defined meaning, with an organic base, in a basic solvent or in at least one inert organic solvent, at 0.degree. C.-50.degree. C., for 1-24 hours;
- (d) converting the COR.sub.1 group of said acylderivative 4 to a carboxylic group, to obtain an acyl D-(+)-carnitine 5 of the formula ##STR6## (e) lactonizing said acyl D-(+)-carnitine 5 to a lactone 6 of L-(-)-carnitine of the formula ##STR7## by treating 5 in a basic environment, and (f) converting said lactone 6 to L-(-)-carnitine inner salt by treating 6 in a basic solution and isolating said L-(-)-carnitine inner salt.
- 2. The process of claim 1, wherein step (d) comprises hydrogenating said acylderivative 4 in an aqueous solution at pH 2-4, at 0.degree. C.-25.degree. C., for 1-8 hours, at 1-4 hydrogen atmospheres, in the presence of a hydrogenation catalyst.
- 3. The process of claim 1, wherein said steps (d), (e) and (f) are carried out as a single step, without isolating said intermediate compounds 5 and 6.
- 4. The process of claim 1, wherein:
- X is a halogen, phosphate, perchlorate, metaperiodate, tetraphenylborate, or alkylsulfonate having 1-12 carbon atoms;
- R.sub.1 is benzyloxy; and
- R is methanesulfonyl (mesyl), p-toluenesulfonyl (tosyl), p-bromobenzenesulfonyl (brosyl), p-nitrobenzenesulfonyl (nosyl), trifluoromethanesulfonyl (triflyl), nonafluoromethanesulfonyl.(nonaflyl) or 2,2,2-trifluoroethansulfonyl (tresyl).
- 5. A process for producing L-(-)-carnitine comprising
- (a) esterifying D-(+)-carnitine to an ester 3 of the general formula ##STR8## wherein R.sub.1 is (i) a straight or branched alkoxy group having 1-11 carbon atoms or (ii) an arylalkoxy or diarylalkoxy group wherein the aryl group is a monocyclic or bicyclic aryl group containing 5 to 12 carbon atoms and the alkyl group has 1-4 carbon atoms, and wherein said arylalkoxy or diarylalkoxy groups can be optionally substituted with a lower alkyl group having 1-4 carbon atoms, an alkoxy group having 1-4 carbon atoms, halogen, a nitro group or an amino group;
- (b) acylating said ester 3 to an acyl derivative 4 of the general formula ##STR9## wherein Y.sup.-, which is the same as or different than X.sup.-, is a counterion imparting solubility to 4 and OR is a leaving group wherein R is selected from an alkylsulfonyl having 1-12 carbon atoms, formyl and trifluoroacetyl,
- by reacting 3 with an acylating agent of the formula RY wherein Y is a halogen or RY is an anhydride and R has the above defined meaning, with an organic base, in a basic solvent or in at least one inert organic solvent, at 0.degree. C.-50.degree. C., for 1-24 hours;
- (c) converting the COR.sub.1 group of said acylderivative 4 to a carboxylic group, to obtain an acyl D-(+)-carnitine 5 of the formula ##STR10## (d) lactonizing said acyl D-(+)-carnitine S to a lactone 6 of L-(-)-carnitine of the formula ##STR11## by treating 5 in a basic environment, and (e) converting said lactone 6 to L-(-)-carnitine by treating 6 in a basic solution and isolating L-(-)-carnitine inner salt.
- 6. The process of claim 5, wherein steps (c), (d), and (e) are carried out as a single step, without isolating said intermediate compounds 5 and 6.
Priority Claims (1)
Number |
Date |
Country |
Kind |
RM92A0915 |
Dec 1992 |
ITX |
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Parent Case Info
This is a division of application Ser. No. 08/170,764 filed on Dec. 21, 1993 now U.S. Pat. No. 5,412,113.
US Referenced Citations (1)
Number |
Name |
Date |
Kind |
4413142 |
Fiorini et al. |
Nov 1983 |
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Divisions (1)
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Number |
Date |
Country |
Parent |
170764 |
Dec 1993 |
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