Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
N-(tert-Butoxycarbonyl)-1,5-diaminopentane → Tert-butyl (5-((2-chloroethyl)sulfonamido)pentyl)carbamate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | N-(tert-Butoxycarbonyl)-1,5-diaminopentane | HCID 4352 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Ethanesulfonylchloride, 2-chloro- | HCID 15385 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | Tert-butyl (5-((2-chloroethyl)sulfonamido)pentyl)carbamate | HCID 86594118 | 100% |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07732441B2 |
| 출처 데이터셋 | uspto-grants-2010_06 |
| ORD ID | ord-617ecb4a7d1545669dc6487048b896de |
| 출처 메모 | uspto-grants-2010_06 |