Sodium Carbonate → ((S)-5-methanesulfonyl-1-methyl-2-oxo-2,3,4,5-tetrahydro-1H-benzo[b][1,4]diazepin-3-yl)-carbamic acid tert-butyl ester

온도

0 °C

A mixture of 623 mg (3.4 mmol) of methanesulfonic acid anhydride and 0.12 ml (0.7 mmol) of N-ethyl-diisopropylamine was cooled to 0° C. and treated with a solution of 200 mg (0.7 mmol) of (S)-(1-methyl-2-oxo-2,3,4,5-tetrahydro-1H-benzo[b][1,4]diazepin-3-yl)-carbamic acid tert-butyl ester in 2 ml of dichloromethane. The reaction mixture was left to warm to room temperature and stirred during 18 h. For the working-up, the reaction mixture was cooled to 0° C. and treated with a saturated solution of sodium carbonate. The organic layer was separated, washed with a saturated solution of ammonium hydrochloride and water, finally dried over sodium sulphate and evaporated. For purification, the crude material was chromatographed on silical gel using a 96:4-mixture of dichloromethane and ethyl acetate as the eluent. There were obtained 100 mg (40% of theory) of the ((S)-5-methanesulfonyl-1-methyl-2-oxo-2,3,4,5-tetrahydro-1H-benzo[b][1,4]diazepin-3-yl)-carbamic acid tert-butyl ester as a white foam;

1. waitThe reaction mixture was left
2. temperatureto warm to room temperature
3. temperaturethe reaction mixture was cooled to 0° C.
4. customThe organic layer was separated
5. washwashed with a saturated solution of ammonium hydrochloride and water
6. dry with materialfinally dried over sodium sulphate
7. customevaporated
8. customFor purification
9. customthe crude material was chromatographed on silical gel

ORD 기록

ord-1a4e553dba4647eca0874b967866b6f1

출처 데이터셋

uspto-grants-2007_01

DOI

10.6084/m9.figshare.5104873.v1

특허 번호

US07160875B2