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

Chlorosulfonyl isocyanate → 6-Bromo-1H-indole-3-carbonitrile

HRID 1027986
노트
인쇄 미리보기

반응식

HRID 1027986 반응식
[Br:1][C:2]1[CH:10]=[C:9]2[C:5]([CH:6]=[CH:7][NH:8]2)=[CH:4][CH:3]=1.ClS([N:15]=[C:16]=O)(=O)=O>CN(C=O)C>[Br:1][C:2]1[CH:10]=[C:9]2[C:5]([C:6]([C:16]#[N:15])=[CH:7][NH:8]2)=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 70918Chlorosulfonyl isocyanateHCID 6764936-Bromoindole

생성물 1

HCID 114700676-Bromo-1H-indole-3-carbonitrile수율 100.2%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

To 6-bromo-1H-indole (41.36 g, 211.0 mmol) in DMF (150 mL) at −78° C. was added chlorosulfonyl isocyanate (20 mL, 225 mmol). After complete addition, the mixture was allowed to warm to room temperature and stirred for 2 hrs. The reaction mixture was poured into ice (500 mL) and stirred for 30 minutes. The precipitate was collected on a filter and dried in a vacuum oven to give 6-bromo-1H-indole-3-carbonitrile as a light-beige solid (46.73 g, 100%).

후처리

  1. additionAfter complete addition
  2. stirringstirred for 30 minutes
  3. customThe precipitate was collected on
  4. filtrationa filter
  5. customdried in a vacuum oven

출처 및 근거

ORD 기록
ord-eadf67fb14f44d17b7dba449aee1e58d
출처 데이터셋
uspto-grants-2014_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08735414B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트