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

N-Iodosuccinimide → 6-Chloro-3-iodoimidazo[1,2-b]pyridazine

HRID 2353049
노트
인쇄 미리보기

반응식

HRID 2353049 반응식
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[N:6]([CH:8]=[CH:9][N:10]=2)[N:7]=1.[I:11]N1C(=O)CCC1=O>C(#N)C>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[N:6]([C:8]([I:11])=[CH:9][N:10]=2)[N:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 120273N-Iodosuccinimide2회HCID 138828Imidazo(1,2-b)pyridazine, 6-chloro-

생성물 1

HCID 532498976-Chloro-3-iodoimidazo[1,2-b]pyridazine수율 69.4%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

14 g of 6-chloroimidazo[1,2-b]pyridazine (Example 1.0) were suspended in 364 ml of acetonitrile, and 20.51 g of N-iodosuccinimide were added. The mixture was stirred at RT for 19 hours. A further 4.31 g of N-iodosuccinimide were added, and the mixture was stirred for 24 hours. The reaction was cooled and the precipitated solid was filtered off with suction, washed with acetonitrile and dried. 17.67 g of the desired product are obtained.

후처리

  1. stirringthe mixture was stirred for 24 hours
  2. temperatureThe reaction was cooled
  3. filtrationthe precipitated solid was filtered off with suction
  4. washwashed with acetonitrile
  5. customdried

출처 및 근거

ORD 기록
ord-64e5ad2189f343bab1c797771545ad9a
출처 데이터셋
uspto-grants-2010_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07750000B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트