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Diisopropylethylamine → 2-Chloro-4-[[(1R,2S)-2-hydroxycyclohexyl]amino]-3-methyl-benzonitrile
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | (1S,2R)-2-aminocyclohexan-1-ol hydrochloride | HCID 17039400 | — |
| 反応物 | 2-Chloro-4-fluoro-3-methylbenzonitrile | HCID 44550971 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 2-Chloro-4-[[(1R,2S)-2-hydroxycyclohexyl]amino]-3-methyl-benzonitrile | HCID 86693784 | 29.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08658693B2 |
| 出典データセット | uspto-grants-2014_02 |
| ORD ID | ord-7392c902ed19404883235588542a6b88 |
| 出典メモ | uspto-grants-2014_02 |