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1-(5-Bromo-3-methylpyridin-2-yl)piperazine → HCID 58484740, 화합물

HRID 2411270
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인쇄 미리보기

반응식

HRID 2411270 반응식
[F:1][C:2]1[CH:10]=[C:9]([CH3:11])[C:5]([C:6]([OH:8])=O)=[CH:4][N:3]=1.[Br:12][C:13]1[CH:14]=[C:15]([CH3:25])[C:16]([N:19]2[CH2:24][CH2:23][NH:22][CH2:21][CH2:20]2)=[N:17][CH:18]=1>>[Br:12][C:13]1[CH:14]=[C:15]([CH3:25])[C:16]([N:19]2[CH2:20][CH2:21][N:22]([C:6]([C:5]3[CH:4]=[N:3][C:2]([F:1])=[CH:10][C:9]=3[CH3:11])=[O:8])[CH2:23][CH2:24]2)=[N:17][CH:18]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 467392701-(5-Bromo-3-methylpyridin-2-yl)piperazineHCID 467392746-Fluoro-4-methylpyridine-3-carboxylic acid

생성물 1

HCID 58484740HCID 58484740, 화합물수율 86.8%

실험 절차

Using 6-fluoro-4-methylnicotinic acid (1.00 g) and 1-(5-bromo-3-methylpyridin-2-yl)piperazine (1.65 g) and by the reaction and treatment in the same manner as in Preparation Example 111, the title compound (2.20 g) was obtained.

후처리

  1. customby the reaction and treatment in the same manner
  2. customas in Preparation Example 111

출처 및 근거

ORD 기록
ord-fab4b36cb0cd42b9b664d2b8db0c9d9a
출처 데이터셋
uspto-grants-2014_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08816079B2

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