Organic compounds -- part of the class 532-570 series – Organic compounds – Heterocyclic carbon compounds containing a hetero ring...
Reexamination Certificate
2000-11-28
2002-02-26
Stockton, Laura L. (Department: 1626)
Organic compounds -- part of the class 532-570 series
Organic compounds
Heterocyclic carbon compounds containing a hetero ring...
C548S154000
Reexamination Certificate
active
06350881
ABSTRACT:
FIELD OF THE INVENTION
The invention particularly relates to an improved process for the preparation of 5-methoxy-4-(methylthioalkyl)-1,3-bis(phenylmethyl)-2-imidazolidone of general formula 2, [wherein R═—CH
2
COCH
2
CH
2
CH
2
COOMe (2a); —CH
2
CH(OMe)
2
(2b); —CH
2
COOMe(2c); —H (2d)] useful for the synthesis of D(+)biotin.
BACKGROUND OF THE INVENTION
Biotin (vitamin H) is one of the B-complex group of vitamins, has immense commercial importance in the area of animal health and nutrition. It is one of the biocatalyst of the reversible metabolic reactions of carbon dioxide transport in micro and macro organisms. It is used in the poultry feed for rapid growth of chicks and healthy hatching of eggs. Biotin-avidin complex finds a vital role in the area of biochemistry.
D(+)-Biotin prepared by the process of the present invention has the formula (4).
D(+)-biotin is prepared in the prior art from amino acids vis., cysteine, cystine and serine. These processes involving L-crystine as the precursor, incorporate intramolecular radical cyclization (E. J. Corey, M. M. Mehorotra,
Tet. Lett.,
29, 57 1988) as the key step is construct the tetrahydrothiophene moiety of biotin.
Another prior art process involves intramolecular cycloaddition (3+2) of derivatives of L-cystine (E. G. Baggiolini, H. L. Lee, G. Pizzolato and M. R. Uskokovic,
J. Am. Chem. Soc.,
104, 6460, 1982), and L-cysteine (H. L. Lee, G. Baggiolini and M. R. Uskokovic,
Tetrahedron
43, 4887, 1987).
In another process starting from L-cysteine, a bicycle imidazolidine is the key intermediate leading to D(+)-biotin (E. Poetsch and M. Casutt, EP 242,686 1986 CA:108:112077k 1988;
Chimia
41, 148, 1987). In a totally different and novel approach, L-cysteine was converted to its thiazolidine derivative which on treatment with bromine is converted stetreospecifically to a bicyclic intermediate as a single stereoisomer and eventually transformed to D(+)-biotin (P. N. Confalone, E. G. Baggioline, D. Lollar, and M. R. Uskokovic,
J. Am. Chem. Soc.,
99, 7020 1977).
Process for stereospecific synthesis of D(+)-Biotin from sugars of suitable configuration are known. [From Mannose
Tet. Lett.,
32, 2765 1975].
The use of L-cysteine in known from U.S. Pat. No. 4,000,972, U.S. Pat. No. 4,130,713, U.S. Pat. No. 4,337,345 and
J. Am. Chem. Soc.,
99, 7020, 1977 avoids the handling of labile intermediate steps but involves 18 steps, in all with the separation of undesired isomer leading to unsatisfactory yields of optically active D(+)-Biotin.
In another process
J. Am. Chem. Soc.,
105, 5946, 1983 and EP 0094776, substituted 3H, 5H-Imidazo[1,5-C]tetra hydro thiazole are described from which after racemate resolution, synthesis of optically active biotin is described.
In another process by Moolenaer, M. J.; Speckamp, W. N.; Hiemstra, H.; Poetsch, E.; Casutt, M.
Angew, Chem., Int. Ed. Engl.
1995, 34, 2391 and DE 3,926,690 involves the intramolecular version of the condensation of a silyl enol ether with N-acyliminium intermediates to effect the ring closure of thio ether to the thiophane nucleus.
In yet another process by Poetsch, E.; Casutt, M., EP 242,686 1986; CA: 108: 112077K 1988;
Chimia
41, 141-150, 1987 describes the formation of keto acid and further elaboration of acid to D(+)-Biotin. The main draw back of this method is use of hazardous 2 eq of diisobutylaluminium hydride (DIBAL-H), Potassium cyanide (KCN), Carbonyldiimidazole and involves reactions to be performed under anhydrous conditions.
In yet another prior art of biotin syntheses by Chavan, S. P.; Chittiboyina, A. G.; Kamat, S. K., Indian Patents NF135/98, 136/98 and Ravindranathan, T.; Chavan, S. P.; Tejwani, R. B. U.S. Pat. No. 5,274,107 (1993) describes the formation of substituted imidazolidines from L-cysteine and further elaboration of hydantoin to D(+)-biotin. This process also involves the use of expensive and hazardous chemicals vis., DIBAL-H, tertiary butyl dimethyl silyl chloride (TBDMSCI), trifluoromethane sulphonic acid (Triflic acid) etc.,
Hiterto known processes involve highly toxic and hazardous chemicals e.g., phosgene for the formation of imidazolidine. Moreover the intramolecular radical cyclization leads to both desired five member as well as undesired six member ring along with tin inclusion compounds as the undesired byproducts.
In another prior art process involving the intramolecular (3+2) cycloaddition reaction of nitrone, the precursor olefin is obtained as a mixture (9:1) of which the desired olefin has to be purified and separated by chromatography. Moreover, the chiral intermediates obtained during the above mentioned sequence of reactions were prone to racemization.
In another prior art process involving the intramolecular cyclization of thiazolidine required Collins oxidation as one of the steps. Use of heavy metals on an industrial scale would lead to problems during waste disposal. Moreover Wittig reaction on the aldehyde leads to a mixture of isomers, which should be separated and the desired isomer subjected to further reactions leading to biotin.
All these processes are however characterized by large number of synthetic steps resulting in low overall yields. The non-crystallizable intermediate stages mostly due to sugar nature are often obtained in impure form and require tedious purification on account of their polyfunctionality and chemical liability connected with it maintenance of comparatively very narrow range of reaction parameters. Additionally these sugars are not easily available in nature which leads to high prices.
In yet another process by Chavan, S. P.; Chittiboyina, A. G.; Kamat, S. K.; Kalkote, U. R.; and Ravindranathan, T. Indian Patents NF 211/00-A, NF 211/00-C describes the formation of 6-Benzyl-7-(1-trimethylsilyloxy-2-oxocyclohexyl)-3-phenyl-(3S, 7R, 7R)-perhydro-imidazo[1,5-C][1,3]thiazole-5-one.
OBJECTS OF THE INVENTION
The object of the present invention is to provide a process for the preparation of 5-methoxy-4-(methylthioalkyl)-1,3-bis(phenylmethyl)-2-imidazolindone having general formula (2a-d), avoiding the use of diisobutylaluminium hydride.
It is another object of the invention to provide a process for the preparation of 5-methoxy-4-(methylthioalkyl)-1,3-bis(phenylmethyl)-2-imidazolidone having general formula (2a-d) which has a good yield.
It is another object of the invention to provide a process for the preparation of 5-methoxy-4-(methylthioalkyl)-1,3-bis(phenylmethyl)-2-imidazolidone having general formula (2-a-d) which does not require substantial subsequent purification after formation, thereby lessening the cost of manufacture.
SUMMARY OF THE INVENTION
Accordingly, the present invention relates to a process for the preparation of 5-methoxy-4-(methylthioalkyl)-1,3-bis(phenylmethyl)-2-imidazolidone having general formula (2a-d)
[wherein R═—CH
2
COCH
2
CH
2
CH
2
COOMe (2a), —CH
2
CH(OMe)
2
(2b); —CH
2
COOMe(2c); —H (2d)] which comprises reacting a reducing agent with 6-benzyl-7-methoxy-3-phenylperhydroimidazo [1,5-c][1.3]thiozol-5-one of general formula (1) in the presence of an organic solvent for a period ranging from 0.5 to 2 hrs at a temperature ranging from −78° C. to 80° C., evaporating the solvent and reacting the residue with an alkylating reagent, optionally in the presence of a phase transfer catalyst and an inorganic base in an organic solvent for a period ranging from 10-12 hrs at room temperature, evaporating the solvent followed by purification to obtain the desired compound of general formula (2a-d).
In one embodiment of the invention, wherein the reducing agent used is a metal or a metal hydride selected from the group consisting of sodium, lithium, tributyltin hydride, potassium in ammonia or ethylenediamine and alkali metal in etheral or hydrocarbon solvent in the present of arene selected from the group consisting of naphthalene, biphenyl and 4,4′-ditertiary butyl alcohol.
In one embodiment of the invention, the organic so
Balakrishnan Kamalam
Chavan Subhash Prataprao
Chittiboyina Amar Gopal
Deshpande Vishnu Hari
Kamat Subhash Krishnaji
Council of Scientific and Industrial Research
Ladas & Perry
Stockton Laura L.
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