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

Methyl trans-4-chloro-2-(phenylsulfonylamino)cinnamate → Methyl[6-chloro-2-[4-(methylsulfonylamino)benzoyl]-1h-indol-3-yl]acetate

HRID 396520
노트
인쇄 미리보기

반응식

HRID 396520 반응식
[Cl:1][C:2]1[CH:13]=[CH:12][C:5](/[CH:6]=[CH:7]/[C:8]([O:10][CH3:11])=[O:9])=[C:4]([NH:14]S(C2C=CC=CC=2)(=O)=O)[CH:3]=1.[CH3:24][S:25]([NH:28][C:29]1[CH:38]=[CH:37][C:32]([C:33](=[O:36])[CH2:34]Br)=[CH:31][CH:30]=1)(=[O:27])=[O:26]>>[CH3:11][O:10][C:8](=[O:9])[CH2:7][C:6]1[C:5]2[C:4](=[CH:3][C:2]([Cl:1])=[CH:13][CH:12]=2)[NH:14][C:34]=1[C:33](=[O:36])[C:32]1[CH:31]=[CH:30][C:29]([NH:28][S:25]([CH3:24])(=[O:27])=[O:26])=[CH:38][CH:37]=1
참가 물질실험 절차출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 11371593Methyl trans-4-chloro-2-(phenylsulfonylamino)cinnamateHCID 15592151N-(4-(2-bromoacetyl)phenyl)methanesulfonamide

생성물 1

HCID 23003240Methyl[6-chloro-2-[4-(methylsulfonylamino)benzoyl]-1h-indol-3-yl]acetate

실험 절차

The title compound was prepared according to the procedure described in Example 8 (Method B) from methyl trans-4-chloro-2-(phenylsulfonylamino)cinnamate (step 1 of Example 8, Method A) and 4-(methylsulfonylamino)phenacyl bromide*.

출처 및 근거

ORD 기록
ord-3695724a4550449891d0cd02ae51c460
출처 데이터셋
uspto-grants-2003_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06608070B1

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차출처 및 근거반응 노트