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Cesium carbonate → HCID 69009937、化合物

HRID 2102410
ノート
印刷プレビュー

反応式

HRID 2102410 の反応式
[F:1][C:2]1[CH:7]=[C:6]([S:8][CH3:9])[CH:5]=[CH:4][C:3]=1[NH2:10].C1(P(C2C=CC=CC=2)C2(P(C3C=CC=CC=3)C3C=CC=CC=3)CC=C3C(C=CC=C3)=C2C2C3C(=CC=CC=3)C=CC=2)C=CC=CC=1.C(=O)([O-])[O-].[Cs+].[Cs+].[CH2:63]([O:65][C:66]([C:68]1[C:73](Cl)=[C:72]([CH3:75])[N:71]2[N:76]=[CH:77][CH:78]=[C:70]2[N:69]=1)=[O:67])[CH3:64]>C1(C)C=CC=CC=1.CCOC(C)=O.C([O-])(=O)C.[Pd+2].C([O-])(=O)C>[CH2:63]([O:65][C:66]([C:68]1[C:73]([NH:10][C:3]2[CH:4]=[CH:5][C:6]([S:8][CH3:9])=[CH:7][C:2]=2[F:1])=[C:72]([CH3:75])[N:71]2[N:76]=[CH:77][CH:78]=[C:70]2[N:69]=1)=[O:67])[CH3:64]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

8

反応物 4

HCID 10796Cesium carbonateHCID 220256172-Fluoro-4-(methylsulfanyl)anilineHCID 69005522HCID 69005522、化合物HCID 86595863(+/-)-2,2-Bis(diphenylphosphino)-1,1-binaphthyl

生成物 1

HCID 69009937HCID 69009937、化合物

試薬・触媒・溶媒 3

HCID 167845
palladium(II) acetate
触媒
HCID 1140Toluene溶媒
HCID 8857Ethyl Acetate溶媒

反応条件

温度
80 °C

実験手順

2-Fluoro-4-methylsulfanyl-phenylamine (1.01 equivalents), palladium(II) acetate (0.10 equivalents), rac-2,2-bis(diphenylphosphino)-1,1′-binaphthyl (0.15 equivalents), and cesium carbonate (1.50 equivalents) are added to a solution of 6-chloro-7-methylpyrazolo[1,5-a]pyrimidine-5-carboxylic acid ethyl ester (1.00 equivalent) in toluene in a sealed vial. After stirring 10 minutes, the mixture is heated to 80° C. After 24 hours, the reaction mixture is cooled to room temperature and diluted with EtOAc. The resulting precipitate is filtered and washed with EtOAc. The filtrate is diluted with EtOAc and washed with water. The aqueous layer is re-extracted with EtOAc. The combined organic layers are washed with brine, dried (MgSO4) and concentrated. The product is purified by flash chromatography as necessary.

後処理

  1. waitAfter 24 hours
  2. temperaturethe reaction mixture is cooled to room temperature
  3. filtrationThe resulting precipitate is filtered
  4. washwashed with EtOAc
  5. additionThe filtrate is diluted with EtOAc
  6. washwashed with water
  7. extractionThe aqueous layer is re-extracted with EtOAc
  8. washThe combined organic layers are washed with brine
  9. dry with materialdried (MgSO4)
  10. concentrationconcentrated
  11. customThe product is purified by flash chromatography as necessary

出典と根拠

ORDレコード
ord-4249cf1c88a745d69eb36390fbdb178a
出典データセット
uspto-grants-2009_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07576072B2

反応ノート

読み込み中…

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