Triethylamine → (4R,5S)-3-(3-isopropylthiopropionyl)-4-methyl-5-phenyl-2-oxazolidinone

226 mg of 3-isopropylthiopropionic acid was dissolved in 1.5 ml of dry dichloromethane. 0.22 ml (1.0 eq) of triethylamine was added thereto, and then the mixture was cooled with ice. 0.19 ml of pivaloyl chloride was added thereto under stirring to obtain a gelled reaction solution. The reaction solution was stirred at 10° C. for 10 minutes and then cooled with ice. A dichloromethane solution of lithium amide prepared from 270 mg of (4R,5S)-4-methyl-5-phenyl-2-oxazolidinone and 0.96 ml of 1.5M n-butyl lithium was prepared, and the solution was added to the previous reaction solution under cooling with ice. The mixture was stirred at room temperature overnight, and then the reaction solution was diluted with 20 ml of chloroform. After washing with 15 ml of a 4% sodium hydrogencarbonate aqueous solution, the chloroform solution was dried over anhydrous magnesium sulfate. The chloroform solution was concentrated under reduced pressure, and then purified by silica gel column chromatography (n-hexane/ethyl acetate=6/1) to obtain 240 mg of (4R,5S)-3-(3-isopropylthiopropionyl)-4-methyl-5-phenyl-2-oxazolidinone as colorless transparent syrup (yield: 51%).

1. temperaturethe mixture was cooled with ice
2. customto obtain a gelled reaction solution
3. stirringThe reaction solution was stirred at 10° C. for 10 minutes
4. temperaturecooled with ice
5. customwas prepared
6. additionthe solution was added to the previous reaction solution
7. temperatureunder cooling with ice
8. stirringThe mixture was stirred at room temperature overnight
9. washAfter washing with 15 ml of a 4% sodium hydrogencarbonate aqueous solution
10. dry with materialthe chloroform solution was dried over anhydrous magnesium sulfate
11. concentrationThe chloroform solution was concentrated under reduced pressure
12. custompurified by silica gel column chromatography (n-hexane/ethyl acetate=6/1)

ORD record

ord-024e6e12d0e3498f85ea4aad3a189ab7

Source dataset

uspto-grants-1996_01

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US05481036