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HRID 526992作成日:2026年10月25日

Triethylamine → benzyl (1S,3R)-3-(4-chlorobutanamido)cyclohexylcarbamate

https://huagongshe.com/reaction/526992

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物4-Chlorobutyryl chlorideHCID 78370—
反応物Benzyl ((1S,3R)-3-aminocyclohexyl)carbamateHCID 69756715—
溶媒DichloromethaneHCID 6344—
生成物benzyl (1S,3R)-3-(4-chlorobutanamido)cyclohexylcarbamateHCID 68101865—

反応手順

To a stirred slurry of benzyl N-[(1S,3R)-3-aminocyclohexyl]carbamate, 18e, (0.97 g, 3.41 mmol) in CH2Cl2 (34 mL), was added Et3N (1.00 mL, 7.15 mmol), followed by 4-chlorobutanoyl chloride (0.40 mL, 3.58 mmol). After stirring at room temperature, the mixture was diluted with CH2Cl2, washed with 1N HCl (2×), 1N NaOH (2×), and brine. The organic layer was dried over Na2SO4, filtered and concentrated in vacuo to give 1.07 g of the desired product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09345708B2
出典データセットuspto-grants-2016_05
ORD IDord-28144edabcba4971b3abc2245a2c7df5
出典メモuspto-grants-2016_05