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Triethylamine → benzyl (1S,3R)-3-(4-chlorobutanamido)cyclohexylcarbamate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 4-Chlorobutyryl chloride | HCID 78370 | — |
| 反応物 | Benzyl ((1S,3R)-3-aminocyclohexyl)carbamate | HCID 69756715 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | benzyl (1S,3R)-3-(4-chlorobutanamido)cyclohexylcarbamate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09345708B2 |
| 出典データセット | uspto-grants-2016_05 |
| ORD ID | ord-28144edabcba4971b3abc2245a2c7df5 |
| 出典メモ | uspto-grants-2016_05 |