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HRID 245075作成日:2026年10月26日

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

https://huagongshe.com/reaction/245075

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物(1S,2R)-2-aminocyclohexan-1-ol hydrochlorideHCID 17039400—
反応物2-Chloro-4-fluoro-3-methylbenzonitrileHCID 44550971—
溶媒DichloromethaneHCID 6344—
生成物2-Chloro-4-[[(1R,2S)-2-hydroxycyclohexyl]amino]-3-methyl-benzonitrileHCID 8669378429.6%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08658693B2
出典データセットuspto-grants-2014_02
ORD IDord-7392c902ed19404883235588542a6b88
出典メモuspto-grants-2014_02