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HRID 7796作成日:2026年10月24日

Dimethylformamide → 4-(cyanomethyl)-N-[(2R)-2-hydroxycyclohexyl]-3-methoxybenzamide

https://huagongshe.com/ja/reaction/7796

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Oxalyl chlorideHCID 65578—
反応物Cyclohexanol, 2-amino-, hydrochloride (1:1), (1R,2R)-HCID 12228412—
反応物4-(Cyanomethyl)-3-methoxybenzoic acidHCID 21990998—
溶媒DichloromethaneHCID 6344—
生成物4-(cyanomethyl)-N-[(2R)-2-hydroxycyclohexyl]-3-methoxybenzamideHCID 69584588—

反応手順

The 4-(cyanomethyl)-3-methoxybenzoic acid (0.33 g, 1.7 mmol) was suspended in anhydrous dichloromethane (5 mL) and treated with oxalyl chloride (0.3 mL, 3.5 mmol) followed by few drops of DMF at 22° C. under argon. After 2 h stirring, the resulting solution was concentrated to dryness, dissolved in dichloromethane (5 mL), and added slowly to a solution of trans-2-aminocyclohexanol hydrochloride (0.26 g, 1.7 mmol) and TEA (0.5 mL, 3.5 mmol) in anhydrous dichloromethane (10 mL). After 20 min stirring, filtered off salt, and concentrated to afford 4-(cyanomethyl)-N-[(2R)-2-hydroxycyclohexyl]-3-methoxybenzamide as a yellow solid. MS (ESI) 289 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07087601B2
出典データセットuspto-grants-2006_08
ORD IDord-8a1abe5c60be4c09bf5242b5d8b1a7a5
出典メモuspto-grants-2006_08