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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 876340생성일: 2026년 10월 24일

1-cyanocyclopropanecarboxylic acid → N-{1-[(1-Cyanocyclopropyl)carbonyl]-5-[4-(trifluoromethyl)phenyl]piperidin-3-yl}benzenecarboxamide

https://huagongshe.com/ko/reaction/876340

반응식

참여 물질

역할이름HCID투입량
반응물1-cyanocyclopropanecarboxylic acidHCID 2733259—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
반응물N-{5-[4-(trifluoromethyl)phenyl]piperidin-3-yl}benzamideHCID 66701397—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DimethylformamideHCID 6228—
생성물N-{1-[(1-Cyanocyclopropyl)carbonyl]-5-[4-(trifluoromethyl)phenyl]piperidin-3-yl}benzenecarboxamideHCID 66761951—

반응 단계

31 mg (0.28 mmol) of 1-cyanocyclopropanecarboxylic acid together with 131 mg (0.34 mmol) of HATU and 56 mg (0.46 mmol) of 4-dimethylaminopyridine were initially charged in 2 ml of DMF, and 80 mg (0.23 mmol) of N-{5-[4-(trifluoromethyl)phenyl]piperidin-3-yl}benzamide were added. The reaction mixture was stirred overnight at RT and then purified by preparative HPLC (Reprosil C18, water/acetonitrile gradient). Yield: 73 mg (72% of theory)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08987248B2
출처 데이터셋uspto-grants-2015_03
ORD IDord-83e81f84ec1a47e0b06d8f17861c1cb5
출처 메모uspto-grants-2015_03