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

N-Iodosuccinimide → 7-chloro-3-iodo-1H-pyrrolo[2,3-c]pyridine

HRID 513204
노트
인쇄 미리보기

반응식

HRID 513204 반응식
[Cl:1][C:2]1[N:3]=[CH:4][CH:5]=[C:6]2[CH:10]=[CH:9][NH:8][C:7]=12.[I:11]N1C(=O)CCC1=O>C(#N)C>[Cl:1][C:2]1[N:3]=[CH:4][CH:5]=[C:6]2[C:10]([I:11])=[CH:9][NH:8][C:7]=12
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 120273N-IodosuccinimideHCID 114350487-Chloro-1H-pyrrolo[2,3-c]pyridine

생성물 1

HCID 534131527-chloro-3-iodo-1H-pyrrolo[2,3-c]pyridine수율 87.6%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

To a mixture of 7-chloro-1H-pyrrolo[2,3-c]pyridine (0.75 g, 4.92 mmol) and N-iodo-succinimide (1.2 g, 5.41 mmol) was added acetonitrile (31 mL) and the solution was heated to 75 C. After 1 h, the mixture was cooled to r.t., the formed solid was filtered, washed with acetonitrile, and dried to yield the title product (1.2 g). HRMS (ESI) calc (M+H)+=278.9180. found 278.9181.

후처리

  1. temperaturethe solution was heated to 75 C
  2. filtrationthe formed solid was filtered
  3. washwashed with acetonitrile
  4. customdried

출처 및 근거

ORD 기록
ord-05e985ae68c94ef9ad62258b38aeeac9
출처 데이터셋
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09102673B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트