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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 68759생성일: 2026년 10월 24일

4-Iodobenzoic acid → 4-[Cyclopropyl-(4-iodo-benzoyl)-amino]-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/ko/reaction/68759

반응식

참여 물질

역할이름HCID투입량
반응물4-Iodobenzoic acidHCID 12085—
반응물DiisopropylethylamineHCID 81531—
반응물O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
반응물tert-Butyl 4-(cyclopropylamino)piperidine-1-carboxylateHCID 2769591—
용매DimethylformamideHCID 6228—
생성물4-[Cyclopropyl-(4-iodo-benzoyl)-amino]-piperidine-1-carboxylic acid tert-butyl esterHCID 68290220—

반응 단계

2-(1H-Benzotriazol-1-yl)-1,1,3,3-tetramethyluronium tetrafluoroborate (2.67 g) is added to a solution of 4-iodo-benzoic acid (2.06 g) and ethyldiisopropylamine (2.88 mL) in N,N-dimethylformamide (15 mL) at room temperature. The solution is stirred for 10 min prior to the addition of 4-cyclopropylamino-piperidine-1-carboxylic acid tert-butyl ester (2.00 g). The resulting mixture stirred at room temperature overnight. The mixture is concentrated in vacuo and the residue is mixed with water and ethyl acetate. The organic phase is separated, washed with water and aqueous NaHCO3 solution, dried, and the solvent is evaporated. The crude product is used for the next reaction step without further purification. LC (method 5): tR=2.32 min; Mass spectrum (ESI+): m/z=471 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822471B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-464cde27ee4d4693b998c15da72b5346
출처 메모uspto-grants-2014_09