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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1951108생성일: 2026년 10월 25일

tert-Butylacetic acid → N-{(3RS,4SR)-4-(3,4-dichloro-phenyl)-1-[1-(1-methyl-cyclopropanecarbonyl)-piperidine-4-carbonyl]-pyrrolidin-3-yl}-3,3,N-trimethyl-butyramide

https://huagongshe.com/reaction/1951108

반응식

참여 물질

역할이름HCID투입량
반응물tert-Butylacetic acidHCID 14057—
반응물[(3SR,4RS)-3-(3,4-Dichloro-phenyl)-4-methylamino-pyrrolidin-1-yl]-[1-(1-methyl-cyclopropanecarbonyl)-piperidin-4-yl]-methanoneHCID 67025815—
생성물N-{(3RS,4SR)-4-(3,4-dichloro-phenyl)-1-[1-(1-methyl-cyclopropanecarbonyl)-piperidine-4-carbonyl]-pyrrolidin-3-yl}-3,3,N-trimethyl-butyramideHCID 67025672—

반응 단계

In analogy to the procedure described for the synthesis of example 97, the title compound N-{(3RS,4SR)-4-(3,4-dichloro-phenyl)-1-[1-(1-methyl-cyclopropanecarbonyl)-piperidine-4-carbonyl]-pyrrolidin-3-yl}-3,3,N-trimethyl-butyramide was prepared from {4-[(3SR,4RS)-3-(3,4-dichloro-phenyl)-4-methylamino-pyrrolidine-1-carbonyl]-piperidin-1-yl}-(1-methyl-cyclopropyl)-methanone using tert-butylacetic acid instead of 4-chloro-3-(trifluoromethyl)benzoic acid and was obtained as a light brown oil. MS m/e: 536.3 [M]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08404679B2
출처 데이터셋uspto-grants-2013_03
ORD IDord-4d946102e4e449209051bf67ee3a67de
출처 메모uspto-grants-2013_03