Bioconversion process for the synthesis of transhydroxy sulfone by Rhodotorula rubra or Rhodotorula piliminae
AssigneeMerck & Co., Inc.
InventorsMichel M. Chartrain, Lorraine G. Katz, Steven A. King
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Abstract
There is disclosed a novel microbial bioconversion process for the synthesis of a trans-hydroxy sulfone intermediate, which is the precursor to topical carbonic anhydrase inhibitors (TCAI's). TCAI's are effective in the treatment of glaucoma and ocular hypertension. The bioconversion process is carried out in the presence of the microorganism Rhodotorula rubra, or Rhodotorula piliminae and results in a trans-hydroxy sulfone which exhibits a diastereomeric excess of greater than 95%.
Claims7
A process for the preparation of a compound of Formula II:
- ##STR9## wherein A is carbon or nitrogen and R.sup.1 is:
- a) C.sub.1-5 alkyl, either straight or branched chain;
- b) C.sub.3-5 alkenyl;
- c) C.sub.3-5 alkynyl;
- d) hydrogen;
- or
- e) C.sub.1-4 alkoxy-C.sub.1-4 alkyl,
- comprising the steps of culturing a microorganism selected from the group consisting of Rhodotorula rubra, ATCC 74283 and Rhodotorula pilirninae ATCC 32762 in a nutrient medium containing assimilable sources of nitrogen and carbon and a substrate of Formula III:
- ##STR10## wherein R.sup.2 is a) C.sub.1-5 alkyl, either straight or branched chain;
- b) C.sub.3-5 alkenyl;
- c) C.sub.3-5 alkynyl;
- d) hydrogen;
- or
- e) C.sub.1-4 alkoxy-C.sub.1-4 alkyl
- under aerobic conditions until a recoverable amount of the compound of Formula II is produced and isolating the compound of Formula II.
A process for the preparation of a compound of Formula II:
- ##STR11## wherein A is carbon or nitrogen and R.sup.1 is:
- C.sub.1-5 alkyl, either straight or branched chain;
- b) C.sub.3-5 alkenyl;
- c) C.sub.3-5 alkynyl;
- d) hydrogen;
- or
- e) C.sub.1-4 alkoxy-C.sub.1-4 alkyl,
- comprising the steps of culturing Rhodotorula rubra, ATCC 74283 in a nutrient medium containing assimilable sources of nitrogen and carbon and a substrate of Formula III:
- ##STR12## wherein R.sup.2 is a) C.sub.1-5 alkyl, either straight or branched chain;
- b) C.sub.3-5 alkenyl;
- c) C.sub.3-5 alkynyl;
- d) hydrogen;
- or
- e) C.sub.1-4 alkoxy-C.sub.1-4 alkyl
- under aerobic conditions until a recoverable amount of the compound of Formula II is produced and isolating the compound of Formula II, wherein the substrate is dissolved in from about 1% to about 15% v/v of ethanol, methanol or DMSO, and the amount of substrate is from about 1 to about 3 g/L, the temperature is from about 20.degree. to about 50.degree. C., and the pH is from about 4.5 to 8.0.
Dependencies are inferred from the claim text.