돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 131966생성일: 2026년 10월 25일

2-Aminothiazole → 1-(2-Cyclopentanesulfonyl-4-methyl-phenyl)-3-thiazol-2-yl-urea

https://huagongshe.com/reaction/131966

반응식

참여 물질

역할이름HCID투입량
반응물2-AminothiazoleHCID 2155—
반응물CyclopentanethiolHCID 15510—
반응물Benzene, 2-fluoro-4-methyl-1-nitro-HCID 67966—
반응물HCID 66998966HCID 66998966—
반응물HCID 66998974HCID 66998974—
생성물1-(2-Cyclopentanesulfonyl-4-methyl-phenyl)-3-thiazol-2-yl-ureaHCID 5973278362%

반응 단계

3-Cyclopentanesulfanyl-4-nitrotoluene (0.83 g, 70%) was prepared from cyclopentyl mercaptan and 3-fluoro-4-nitrotoluene (0.77 g, 5.0 mmol) following the general procedure A. This was oxidized to 3-cyclopentanesulfonyl-4-nitrotoluene (0.84 g, 90%) following general procedure R. 3-Cyclopentanesulfonyl-4-nitrotoluene was reduced to 2-cyclopentanesulfonyl-4-methyl-aniline (0.53 g, 70%) following general procedure C. 1-(2-Cyclopentanesulfonyl-4-methyl-phenyl)-3-thiazol-2-yl-urea (225 mg, 62%) was prepared from 2-cyclopentanesulfonyl-4-methyl-aniline (239 mg, 1.0 mmol) and 2-aminothiazole (100 mg, 1.0 mmol) following the general procedure D.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07384967B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-a3b40849388c4b1abe1d6cc9acfc9eba
출처 메모uspto-grants-2008_06