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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 68883생성일: 2026년 10월 25일

N-methyl-2-pyrrolidone → N-Cyclopropyl-N-[1-(5-cyclopropyl-pyrimidin-2-yl)-piperidin-4-yl]-4-oxazol-5-yl-benzamide

https://huagongshe.com/reaction/68883

반응식

참여 물질

역할이름HCID투입량
반응물N-methyl-2-pyrrolidoneHCID 13387—
반응물2-((1,1-Dimethylethyl)imino)-N,N-diethylhexahydro-1,3-dimethyl-2lambda5-1,3,2-diazaphosphorin-2-amineHCID 3513851—
반응물2-Chloro-5-cyclopropylpyrimidineHCID 46864087—
반응물N-cyclopropyl-4-oxazol-5-yl-N-piperidin-4-yl-benzamide hydrochlorideHCID 68289930—
생성물N-Cyclopropyl-N-[1-(5-cyclopropyl-pyrimidin-2-yl)-piperidin-4-yl]-4-oxazol-5-yl-benzamideHCID 68290561—

반응 조건

온도70 °C

반응 단계

A mixture of N-cyclopropyl-4-oxazol-5-yl-N-piperidin-4-yl-benzamide hydrochloride (35 mg), 2-chloro-5-cyclopropyl-pyrimidine (46 mg), and 2-tert-butylimino-2-diethylamino-1,3-dimethyl-perhydro-1,3,2-diazaphosphorine (82 mg) in N-methylpyrrolidinone (1.5 mol) is stirred at 70° C. overnight. The crude product is purified by preparative HPLC to give the title compound. LC (method 18): tR=1.41 min; Mass spectrum (ESI+): m/z=430 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822471B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-9e651429f62d4195bb16b465012fff3f
출처 메모uspto-grants-2014_09