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

Methyl iodide → 6-Chloro-5-iodo-2-(methylthio)-1H-benzo[d]imidazole

HRID 340766
노트
인쇄 미리보기

반응식

HRID 340766 반응식
C([O-])([O-])=O.[K+].[K+].I[CH3:8].[Cl:9][C:10]1[C:19]([I:20])=[CH:18][C:13]2[NH:14][C:15](=[S:17])[NH:16][C:12]=2[CH:11]=1>CC(C)=O>[Cl:9][C:10]1[C:19]([I:20])=[CH:18][C:13]2[N:14]=[C:15]([S:17][CH3:8])[NH:16][C:12]=2[CH:11]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6328Methyl iodide2회HCID 11430Potassium Carbonate2회HCID 574814685-Chloro-6-iodo-1H-benzo[d]imidazole-2(3H)-thione

생성물 1

HCID 574814886-Chloro-5-iodo-2-(methylthio)-1H-benzo[d]imidazole

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

K2CO3 (0.22 g, 1.61 mmol), followed by iodomethane (0.1 mL, 1.61 mmol), was added to a solution of 5-chloro-6-iodo-1,3-dihydro-2H-benzimidazole-2-thione (1 g, 3.22 mmol) in acetone (20 mL) at 0° C. The reaction was stirred at rt for 1 h. Additional K2CO3 (1.61 mmol) and iodomethane (1.61 mmol) were added. The reaction was stirred at rt overnight, then the volatiles were removed and the residue was partitioned between EtOAc and water. Concentration of the EtOAc layer afforded the desired product as a white foam, which was used in the next step without further purification.

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

후처리

  1. stirringThe reaction was stirred at rt overnight
  2. customthe volatiles were removed
  3. customthe residue was partitioned between EtOAc and water

출처 및 근거

ORD 기록
ord-813520244f8f4eb3825465972b17b708
출처 데이터셋
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08895596B2

반응 노트

불러오는 중…