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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 894095생성일: 2026년 10월 24일

Butylurea → N-(4-[2-(1-oxo-isoindoline-2-carboxamido)-ethyl]-benzenesulfonyl)-N'-butyl-urea

https://huagongshe.com/ko/reaction/894095

반응식

참여 물질

역할이름HCID투입량
반응물ButylureaHCID 11595—
반응물Sodium hydrideHCID 24758—
반응물4-[2-(1-Oxo-isoindoline-2-carboxamido)-ethyl]-benzene sulfochlorideHCID 21162349—
용매TetrahydrofuranHCID 8028—
생성물N-(4-[2-(1-oxo-isoindoline-2-carboxamido)-ethyl]-benzenesulfonyl)-N'-butyl-ureaHCID 21162325—

반응 단계

4.8 g of butyl urea are dissolved in 100 ml of tetrahydrofurane and, while stirring, 1.5 g of 80% sodium hydride (in oil) are added. The mixture is heated for 3 hours to 60° C. whereupon 7.6 g of 4-[2-(1-oxo-isoindoline-2-carboxamido)-ethyl]-benzene-sulfochloride in 100 ml of tetrahydrofurane are added while cooling. The temperature is slowly raised to 60°-70° C. and stirring is continued at that temperature for 3 hours. The solvent is removed under reduced pressure, water is added to the residue, the mixture is filtered and the filtrate is acidified with dilute hydrochloric acid. After recrystallization from dilute acetone, the N-(4-[2-(1-oxo-isoindoline-2-carboxamido)-ethyl]benzenesulfonyl)-N'-butyl-urea melts at 189°-190° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04282239
출처 데이터셋uspto-grants-1981_08
ORD IDord-eeaef196eedc4b268efebd985dfcd232
출처 메모uspto-grants-1981_08