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N-(tert-Butoxycarbonyl)-1,5-diaminopentane → Tert-butyl (5-((2-chloroethyl)sulfonamido)pentyl)carbamate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | N-(tert-Butoxycarbonyl)-1,5-diaminopentane | HCID 4352 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Ethanesulfonylchloride, 2-chloro- | HCID 15385 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | Tert-butyl (5-((2-chloroethyl)sulfonamido)pentyl)carbamate | HCID 86594118 | 100% |
反応手順
To a stirred solution of 5-(tert-butoxycarbonylamino)pentylamine (1.00 g, 4.94 mmol) and triethylamine (689 μL g, 4.94 mmol) in dichloromethane (22 mL) at 0° C. was added 2-chloro-1-ethanesulfonyl chloride (470 μL, 4.50 mmol). The reaction mixture was stirred for 2 h at room temperature and then washed with saturated aqueous sodium bicarbonate solution (15 mL). The organic layer was dried (Na2SO4) and the solvent was removed under reduced pressure to give the title compound (100% yield), which was used in the next step without further purification.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07732441B2 |
| 出典データセット | uspto-grants-2010_06 |
| ORD ID | ord-617ecb4a7d1545669dc6487048b896de |
| 出典メモ | uspto-grants-2010_06 |