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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 245075생성일: 2026년 10월 26일

Diisopropylethylamine → 2-Chloro-4-[[(1R,2S)-2-hydroxycyclohexyl]amino]-3-methyl-benzonitrile

https://huagongshe.com/reaction/245075

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물(1S,2R)-2-aminocyclohexan-1-ol hydrochlorideHCID 17039400—
반응물2-Chloro-4-fluoro-3-methylbenzonitrileHCID 44550971—
용매DichloromethaneHCID 6344—
생성물2-Chloro-4-[[(1R,2S)-2-hydroxycyclohexyl]amino]-3-methyl-benzonitrileHCID 8669378429.6%

반응 단계

A mixture of 2-chloro-4-fluoro-3-methyl-benzonitrile (500 mg, 2.95 mmol), diisopropylethylamine (1.29 mL, 7.37 mmol), and (1S,2R)-2-aminocyclohexanol hydrochloride (670 mg, 4.42 mmol, Acros®) is microwaved using a CEM® microwave at 190° C. for 2 h and 180° C. for 4 h. The mixture is diluted with dichloromethane and washed with 1 N HCl. The aqueous layer is extracted again with dichloromethane. The combined organic phases are dried over sodium sulfate, filtered, and concentrated in vacuo. The resulting residue is purified using radial chromatography, eluting with 2% methanol/dichloromethane. The isolated product is recrystallized with ether and hexane to yield the title compound as a white solid (231 mg, 29%). LC-ES/MS m/z 265.0 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08658693B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-7392c902ed19404883235588542a6b88
출처 메모uspto-grants-2014_02