돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 598913생성일: 2026년 10월 25일

2-Aminothiazole → 2-[([[(2-Phenoxyanilino)sulfonyl]amino]carbonyl)amino]thiazole

https://huagongshe.com/reaction/598913

반응식

참여 물질

역할이름HCID투입량
반응물2-AminothiazoleHCID 2155—
반응물Chlorosulfonyl isocyanateHCID 70918—
반응물Benzenamine, 2-phenoxy-HCID 75899—
반응물DiisopropylethylamineHCID 81531—
용매TetrahydrofuranHCID 8028—
생성물2-[([[(2-Phenoxyanilino)sulfonyl]amino]carbonyl)amino]thiazoleHCID 5973284566.6%

반응 조건

온도0 °C

반응 단계

To a solution of chlorosulfonyl isocyanate (0.22 ml, 2.5 mmol) in tetrahydrofuran (25 ml) were added 2-phenoxyaniline (0.37 g, 2.0 mmol) and DIEA (0.89 ml, 5.0 mmol) at −78° C. The solution was stirred and slowly allowed to warmed up to 0° C. To this reaction mixture, was added 2-amino thiazole (0.20 g, 2.0 mmol) and continued stirring at room temperature for 3 h. The reaction mixture was concentrated under reduced pressure and the crude product was purified by column chromatography (ethylacetate:hexanes, from 50:50 to 90:10 as eluent system) to afford the title compound (0.52 g, 66%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07897628B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-a88826546f7f44079a87de659a2038dc
출처 메모uspto-grants-2011_03