홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

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

HRID 131966
노트
인쇄 미리보기

반응식

HRID 131966 반응식
[CH:1]1([SH:6])CCC[CH2:2]1.FC1C=C(C)C=CC=1[N+]([O-])=[O:15].[CH:18]1([S:23]([C:26]2[CH:27]=[C:28]([CH3:35])[CH:29]=[CH:30][C:31]=2[N+:32]([O-])=O)(=[O:25])=[O:24])[CH2:22][CH2:21][CH2:20][CH2:19]1.C1(S(C2C=C(C)C=CC=2N)(=O)=O)CCCC1.[NH2:52][C:53]1SC=[CH:56][N:57]=1>>[CH:18]1([S:23]([C:26]2[CH:27]=[C:28]([CH3:35])[CH:29]=[CH:30][C:31]=2[NH:32][C:56]([NH:57][C:53]2[S:6][CH:1]=[CH:2][N:52]=2)=[O:15])(=[O:25])=[O:24])[CH2:22][CH2:21][CH2:20][CH2:19]1
참가 물질실험 절차출처 및 근거반응 노트

참가 물질

6

반응물 5

HCID 21552-AminothiazoleHCID 15510CyclopentanethiolHCID 67966Benzene, 2-fluoro-4-methyl-1-nitro-HCID 669989663-Cyclopentanesulfonyl-4-nitrotoluene2회HCID 669989742-Cyclopentanesulfonyl-4-methyl-phenylamine2회

생성물 1

HCID 59732783
1-(2-Cyclopentanesulfonyl-4-methyl-phenyl)-3-thiazol-2-yl-urea
수율 62%

실험 절차

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

ORD 기록
ord-a3b40849388c4b1abe1d6cc9acfc9eba
출처 데이터셋
uspto-grants-2008_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07384967B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차출처 및 근거반응 노트