돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 225964생성일: 2026년 10월 26일

Triethylamine → methyl [(2S,4EZ)-1-(biphenyl-4-yl-carbonyl)--4-(methoxyimino)pyrrolidin-2-yl]acetate

https://huagongshe.com/reaction/225964

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물O-methylhydroxylammonium chlorideHCID 11639—
반응물methyl [(2S)-1-(biphenyl-4-ylcarbonyl)-4-oxopyrrolidin-2-yl]acetateHCID 86760911—
용매ChloroformHCID 6212—
용매DichloromethaneHCID 6344—
생성물methyl [(2S,4EZ)-1-(biphenyl-4-yl-carbonyl)--4-(methoxyimino)pyrrolidin-2-yl]acetateHCID 13172752684%

반응 단계

A solution of methyl [(2S)-1-(biphenyl-4-ylcarbonyl)-4-oxopyrrolidin-2-yl]acetate (43 mg, 0.13 mmol), hydroxylamine methyl ether hydrochloride (32 mg, 0.38 mmol) and triethylamine (53 μl, 0.38 mmol) in chloroforme (3 ml) was stirred at 70° C. for 5 days. The reaction mixture was diluted with dichloromethane and washed with HCl 1N. The organic phase was dried (MgSO4) and concentrated to afford methyl [(2S,4EZ)-1-(biphenyl-4-yl-carbonyl)--4-(methoxyimino)pyrrolidin-2-yl]acetate (40 mg). Yield: 62%. HPLC purity: 94%

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07557136B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-fd74bb2257964a56a4a9068902b53e9a
출처 메모uspto-grants-2009_07