Process for preparing optically active carnitine ester

Details Process for preparing optically active carnitine ester Process for preparing optically active carnitine ester

1993-10-22

2001-03-06

Reamer, James H. (Department: 1614)

Organic compounds -- part of the class 532-570 series

Organic compounds

Carboxylic acid esters

Reexamination Certificate

active

06197996

ABSTRACT:

FIELD OF THE INVENTION
This invention relates to a process for preparing an optically active carnitine ester which is an intermediate for obtaining medicinally important optically active carnitine. More particularly, it relates to a process for preparing an optically active carnitine ester by asymmetric hydrogenation of a &ggr;-trimethylammonium-3-oxobutanoic ester halide in the presence of a ruthenium-optically active phosphine complex as a catalyst.
BACKGROUND OF THE INVENTION
L-Carnitine is present in a living body and functions to carry activated long-chain free fatty acids through the mitochondrial inner membrane. Acyl-CoA derivatives are allowed to enter into the mitochondrial matrix through the mitochondrial inner membrane only in the form of their ester with L-carnitine. Such a carrier function of L-carnitine is exerted in derivering the activated long-chain fatty acids from the site of their biosynthesis. The carnitine found in the living body is exclusively levorotatory, i.e., of L-form, while D-carnitine has never been detected in living bodies.
On the other hand, racemic carnitine has been used for years for various purposes. For example, DL-carnitine has been sold in Europe as an appetizer and also reported to have an effect of promoting physical development of children as described in Borniche et al.,
Olinioa Chemica Acta
, Vol. 5, pp. 171 to 176 (1960). However, in recent years, an importance of using only L-carnitine for therapeutic purposes has been increasing. That is, D-carnitine has turned out to antagonize against carnitine acyltransferase, e.g., carnitine acetyl transferase (CAT) and carnitine palmitoyl transferase (PTC). It has also been elucidated recently that D-carnitine causes depletion of L-carnitine in cardiac tissues. Accordingly, it is essential that cases under treatment for cardiac diseases or for reduction of blood fat should receive only L-carnitine. L-carnitine has thus been recognized as an important medicine.
Known techniques for preparing an optically active carnitine ester and carnitine include (i) optical resolution of a racemate, (ii) biochemical reduction of the corresponding keto ester, and (iii) synthesis using other optically active substances as a starting material or an intermediate.
Examples of the technique (i) include a process in which DL-carnitine amide hydrochloride is subjected to an ion exchange treatment and then resolved using D-camphoric acid as disclosed in JP-A-55-13299 (the term “JP-A” as used herein means an “unexamined published Japanese patent application”) and a process in which DL-carnitine nitrile is resolved using L-camphor-10-sulfonic acid as disclosed in JP-B-40-3891 (the term “JP-B” as used herein means an “examined published Japanese patent application”). Examples of the technique (ii) include a process in which a &ggr;-halo-acetoacetic ester is converted to an optically active &ggr;-halo-&bgr;-hydroxybutyric ester by microbial fermentation and then quaternarized with trimethylamine as disclosed in JP-A-59-118093 and a process in which &ggr;-azidoacetoacetic ester is reduced with a microorganism to obtain an optically active &ggr;-azido-&bgr;-hydroxybutyric ester. Examples of the technique (iii) include a process using D-mannitol as disclosed in JP-A-57-165352 and a process using (S)-chloromethyloxirane as disclosed in JP-A-62-212382.
However, the processes (i) utilizing resolution of a racemate as a carnitine precursor require a resolving agent in an amount equimolar to the substrate. Also, the highest possible yield of the desired product, attained if the reaction ideally proceeds, is 50%. Namely, the undesired enantiomer is useless or must be racemized for re-use. The processes (ii) utilizing microbial asymmetric reduction are disadvantageous in that the usable substrate is limited, the production efficiency is low in many cases, and isolation of the product from the reaction solution involves complicated procedures. The processes (iii) using a naturally-occuring optically active substance as a starting material have disadvantages, such as requirement of long reaction steps.
SUMMARY OF THE INVENTION
As a result of extensive investigations with the purpose of settling the above-described problems, the inventors have found that a carnitine ester having high optical purity can be obtained in good yield by quaternarizing a &ggr;-haloacetacetic ester with trimethylamine followed by asymmetric hydrogenation in the presence of a rhuthenium-optically active phosphine complex as a catalyst.
The present invention relates to a process for preparing an optically active carnitine ester represented by formula (I):
wherein R represents a lower alkyl group; and X represents a halogen atom,
which comprises asymmetrically hydrogenating a &ggr;-trimethylammonium-3-oxobutanoic ester halide represented by formula (II):
wherein R and X are as defined above,
in the presence of a ruthenium-optically active phosphine complex as a catalyst.
DETAILED DESCRIPTION OF THE INVENTION
The compound represented by formula (II) which can be used in the present invention as a starting material can easily be synthesized by, for example, the process described in JP-A-51-63123.
In formula (II), the lower alkyl group as represented by R includes those containing from 1 to 4 carbon atoms, such as methyl, ethyl, butyl, n-propyl, isopropyl, isobutyl, and t-butyl groups; and the halogen atom as represented by X includes chlorine, bromine, and iodine atoms.
Examples of suitable ruthenium-optically active phosphine complexes which can be used for asymmetric hydrogenation, include those represented by formulae (III), (V), (VI), and (VII):
Ru
x
H
y
Cl
z
(R
1
—BINAP)
2
(Q)
p
  (III)
wherein R
1
—BINAP represents a tertiary phosphine represented by formula (IV):
R
1
represents a hydrogen atom, a methyl group or a t-butyl group; Q represents a tertiary amine; when y is 0, then x represents 2, z represents 4, and p represents 1; and when y is 1, then x represents 1, z represents 1, and p represents 0,
[RuH
u
(R
1
—BINAP)
v
]Y
w
  (V)
wherein R
1
—BINAP is as defined above; Y represents ClO
4
, BF
4
or PF
6
; when us is 0, then v represents 1, and w represents 2; and when u is 1, then v represents 2, and w represents 1,
wherein R
1
—BINAP is as defined above; and R
2
represents a lower alkyl group (such as those containing from 1 to 4 carbon atoms) or a trifluoromethyl group, and
[Ru(R
1
—BINAP)MCl
k
]
l
X
1
m
  (VII)
wherein R
1
—BINAP is as defined above; M represents Zn, Al, Ti or Sn; X
1
represents N(C
2
H
5
)
3
or CH
3
CO
2
; in the case that X
1
represents N(C
2
H
5
)
3
, l is 2 and m is 1, and when M represents Zn, then k is 4, when M represents Al, then k is 5, and when M represents Ti or Sn, then k is 6; and in the case that X
1
represents CH
3
CO
2
, l is 1 and m is 2, and when M represents Zn, then k is 2, when M represents Al, then k is 3, and when M represents Ti or Sn, then k is 4.
The ruthenium-optically active phosphine complex represented by formula (III) can be obtained by the process disclosed in T. Ikariya et al.,
J. Chem. Soc., Chem. Commun.,
922-924 (1985) and JP-A-61-63690.
The complexes represented by formulae (V) and (VI) can be obtained by the processes disclosed in JP-A-63-41487 JP-A-62-265293, respectively.
The complex represented by formula (VII) can be obtained by starting with Ru
2
Cl
4
(R
1
—BINAP)
2
(NEt
3
) (wherein Et represents an ethyl group, hereinafter the same), one of the complexes of formula (III), or Ru(R
1
—BINAP)(OCOCH
3
)
2
, or one of the complexes of formula (VI). That is, Ru
2
Cl
4
(R
1
—BINAP)
2
(NEt
3
) or Ru(R
1
—BINAP)(OCOCH
3
)
2
is reacted with a Lewis acid selected from zinc chloride, aluminum chloride, titanium tetrachloride, and tin tetrachloride in a solvent, e.g., methylene chloride, at a temperature of from 10 to 25° C. for a period of from 2 to 20 hours, and the solvent is removed from the reaction mixture by distillation, followed by drying to obtain the desired ruthenium-optically active phosphine complex as a solid.
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