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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 14448생성일: 2026년 10월 25일

N-(tert-Butoxycarbonyl)-1,5-diaminopentane → Tert-butyl (5-((2-chloroethyl)sulfonamido)pentyl)carbamate

https://huagongshe.com/reaction/14448

반응식

참여 물질

역할이름HCID투입량
반응물N-(tert-Butoxycarbonyl)-1,5-diaminopentaneHCID 4352—
반응물TriethylamineHCID 8471—
반응물Ethanesulfonylchloride, 2-chloro-HCID 15385—
용매DichloromethaneHCID 6344—
생성물Tert-butyl (5-((2-chloroethyl)sulfonamido)pentyl)carbamateHCID 86594118100%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732441B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-617ecb4a7d1545669dc6487048b896de
출처 메모uspto-grants-2010_06