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

N-(2-amino-phenyl)-5-bromo-2-fluoro-benzamide → 2-(5-Bromo-2-fluoro-phenyl)-1H-benzoimidazole

HRID 2047388
노트
인쇄 미리보기

반응식

HRID 2047388 반응식
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[NH:8][C:9](=O)[C:10]1[CH:15]=[C:14]([Br:16])[CH:13]=[CH:12][C:11]=1[F:17]>C(O)(=O)C>[Br:16][C:14]1[CH:13]=[CH:12][C:11]([F:17])=[C:10]([C:9]2[NH:8][C:3]3[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=3[N:1]=2)[CH:15]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 24693313N-(2-amino-phenyl)-5-bromo-2-fluoro-benzamide

생성물 1

HCID 432364512-(5-Bromo-2-fluoro-phenyl)-1H-benzoimidazole수율 89.3%

시약·촉매·용매 1

HCID 176Acetic Acid용매

반응 조건

온도
60 °C

실험 절차

A suspension of N-(2-amino-phenyl)-5-bromo-2-fluoro-benzamide (5.64 g, 18.3 mmol) in acetic acid (20 mL) was heated at 60° C. After 30 min, the suspension became a solution and it was left overnight. The solvent was removed under reduced pressure and residue was triturated with DCM (10 mL) and filtered off. The precipitate was washed with DCM (3×10 mL) and dried to afford 4.76 g of the title compound (89%).

후처리

  1. waitwas left overnight
  2. customThe solvent was removed under reduced pressure and residue
  3. customwas triturated with DCM (10 mL)
  4. filtrationfiltered off
  5. washThe precipitate was washed with DCM (3×10 mL)
  6. customdried

출처 및 근거

ORD 기록
ord-a0020226a2894bd2a1ecc68c4a8d1139
출처 데이터셋
uspto-grants-2013_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08592463B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트