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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 225962생성일: 2026년 10월 24일

Triethylamine → [(2S,4EZ)-1-(biphenyl-4-ylcarbonyl)-4-(methoxyimino)pyrrolidin-2-yl] acetic acid

https://huagongshe.com/ko/reaction/225962

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물O-methylhydroxylammonium chlorideHCID 11639—
반응물[(2s)-1-(Biphenyl-4-ylcarbonyl)-4-oxopyrrolidin-2-yl]acetic acidHCID 69036428—
용매ChloroformHCID 6212—
생성물[(2S,4EZ)-1-(biphenyl-4-ylcarbonyl)-4-(methoxyimino)pyrrolidin-2-yl] acetic acidHCID 13172752548.7%

반응 단계

A solution of [(2S)-1-(biphenyl-4-ylcarbonyl)-4-oxopyrrolidin-2-yl]acetic acid (Intermediate 5, 1.50 g, 6.64 mmol), hydroxylamine methyl ether hydrochloride (0.58 g, 6.96 mmol) and triethylamine (1.62 ml, 11.60 mmol) in chloroforme (30 ml) was stirred at RT for 2 days Solvent was removed under reduced pressure and the residue was taken up in ethyl acetate. Organic phase was washed twice with a solution of citric acid 10% and once with brine. Organic phase was then dried on MgSO4, filtered, and concentrated to give [(2S,4EZ)-1-(biphenyl-4-ylcarbonyl)-4-(methoxyimino)pyrrolidin-2-yl]acetic acid as a cream solid (1.14 g). Yield: 45%. HLPC purity: 92%

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07557136B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-5a0a347e841840a688139dd8ff711e73
출처 메모uspto-grants-2009_07