돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1022663생성일: 2026년 10월 27일

Acetic Acid → tert-butyl (6SR,7SR)-6-amino-7-(3,4-dichlorophenyl)-1,4-oxazepane-4-carboxylate

https://huagongshe.com/reaction/1022663

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물2,2'-BipyridineHCID 1474—
반응물Sodium borohydrideHCID 4311764—
반응물tert-butyl (6SR,7SR)-6-azido-7-(3,4-dichlorophenyl)-1,4-oxazepane-4-carboxylateHCID 86663863—
촉매Cobalt dibromideHCID 24610—
용매EthanolHCID 702—
생성물tert-butyl (6SR,7SR)-6-amino-7-(3,4-dichlorophenyl)-1,4-oxazepane-4-carboxylateHCID 6697529975.8%

반응 조건

온도2.5 °C

반응 단계

To a solution of cobalt bromide (15 mg) in ethanol (5 mL) was added 2,2′-bipyridyl (33 mg), sodium tetrahydroborate (53 mg) was added, and the mixture was stirred at 0-5° C. for 5 min. To the reaction mixture was added a solution of tert-butyl (6SR,7SR)-6-azido-7-(3,4-dichlorophenyl)-1,4-oxazepane-4-carboxylate (270 mg) in ethanol (5 mL), and the mixture was stirred at 0-5° C. for 30 min. Acetic acid was added to the reaction mixture, and the mixture was stirred at room temperature for 5 min. The solvent was evaporated under reduced pressure. The residue was neutralized with saturated aqueous sodium hydrogen carbonate, and the mixture was extracted with ethyl acetate. The extract was washed with brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography to give the title compound (191 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08722662B2
출처 데이터셋uspto-grants-2014_05
ORD IDord-1253be1d357643009d53a3f1f5bbcd89
출처 메모uspto-grants-2014_05