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

2-(4-Fluoro-5-nitrobenzoyl)-3-methylpyridine → 3-Amino-4-fluorophenyl 3-methyl-2-pyridyl ketone

HRID 48974
노트
인쇄 미리보기

반응식

HRID 48974 반응식
[F:1][C:2]1[C:16]([N+:17]([O-])=O)=[CH:15][C:5]([C:6]([C:8]2[C:13]([CH3:14])=[CH:12][CH:11]=[CH:10][N:9]=2)=[O:7])=[CH:4][CH:3]=1>[Fe].C(O)(=O)C>[CH3:14][C:13]1[C:8]([C:6]([C:5]2[CH:4]=[CH:3][C:2]([F:1])=[C:16]([NH2:17])[CH:15]=2)=[O:7])=[N:9][CH:10]=[CH:11][CH:12]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 206342552-(4-Fluoro-5-nitrobenzoyl)-3-methylpyridine

생성물 1

HCID 120568333-Amino-4-fluorophenyl 3-methyl-2-pyridyl ketone수율 73.4%

시약·촉매·용매 2

HCID 23925Iron촉매HCID 176Acetic Acid용매

실험 절차

To a mixture of 2-(4-fluoro-5-nitrobenzoyl)-3-methylpyridine (7.13 g, 0.0258 mol) and glacial acetic acid at 70-80° C. is added iron powder (7.76 g, 0.130 mol) in three portions. The resultant mixture is stirred overnight at 70-80° C., cooled to room temperature and extracted three times with ethyl acetate. The combined organic layers are filtered through Celite, dried over anhydrous magnesium sulfate and concentrated in vacuo to afford the title compound as a tan solid (4.36 g, 69.8%) which is identified by NMR spectral analysis.

후처리

  1. extractionextracted three times with ethyl acetate
  2. filtrationThe combined organic layers are filtered through Celite
  3. dry with materialdried over anhydrous magnesium sulfate
  4. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-0a960065e0924f689f305d413ebcea84
출처 데이터셋
uspto-grants-2004_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06706663B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트