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Water → HCID 67500172, 화합물

HRID 921553
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HRID 921553 반응식
F[C:2]1[CH:9]=[CH:8][C:5]([C:6]#[N:7])=[CH:4][C:3]=1[CH3:10].C(=O)([O-])[O-].[Cs+].[Cs+].[F:17][C:18]([F:39])([F:38])[C:19]1[C:27]2[C:22](=[N:23][CH:24]=[CH:25][C:26]=2[C:28]2[CH:29]=[N:30][C:31]3[C:36]([CH:37]=2)=[CH:35][CH:34]=[CH:33][CH:32]=3)[NH:21][N:20]=1.O>CN1CCCC1=O>[CH3:10][C:3]1[CH:4]=[C:5]([CH:8]=[CH:9][C:2]=1[N:21]1[C:22]2=[N:23][CH:24]=[CH:25][C:26]([C:28]3[CH:29]=[N:30][C:31]4[C:36]([CH:37]=3)=[CH:35][CH:34]=[CH:33][CH:32]=4)=[C:27]2[C:19]([C:18]([F:17])([F:39])[F:38])=[N:20]1)[C:6]#[N:7]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 10796Cesium carbonateHCID 27791804-Fluoro-3-methylbenzonitrileHCID 178506293HCID 178506293, 화합물

생성물 1

HCID 67500172HCID 67500172, 화합물수율 11%

시약·촉매·용매 1

HCID 13387N-methyl-2-pyrrolidone용매2회

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온도
120 °C

실험 절차

4-Fluoro-3-methylbenzonitrile (0.052 g) and cesium carbonate (0.150 g) were added to a solution of compound (1d) (0.092 g) in 1-methyl-2-pyrrolidone (hereinafter referred to as NMP) (1.0 mL), followed by stirring at 120° C. for 60 hr. Water was added to the reaction solution, and the precipitate was collected by filtration and was washed by sprinkling water to obtain 3-methyl-4-{4-(quinolin-3-yl)-3-(trifluoromethyl)-1H-pyrazolo[3,4-b]pyridin-1-yl}benzonitrile (11%). According to Example 1(7), compound (82) (64%) was prepared as a white solid using 3-methyl-4-{4-(quinolin-3-yl)-3-(trifluoromethyl)-1H-pyrazolo[3,4-b]pyridin-1-yl}benzonitrile instead of compound (1f).

후처리

  1. filtrationthe precipitate was collected by filtration
  2. washwas washed

출처 및 근거

ORD 기록
ord-f3cee51dfbe8474b8a9702ea35a0035b
출처 데이터셋
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09273045B2

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