Cesium carbonate → [3-(5-Bromo-2-chloro-pyrimidin-4-yloxy)-cyclobutyl]-carbamic acid tert-butyl ester

HRID 1846824ノート

反応式

HRID 1846824 の反応式
[C:1]([O:5][C:6](=[O:13])[NH:7][CH:8]1[CH2:11][CH:10]([OH:12])[CH2:9]1)([CH3:4])([CH3:3])[CH3:2].C([O-])([O-])=O.[Cs+].[Cs+].[Br:20][C:21]1[C:22](Cl)=[N:23][C:24]([Cl:27])=[N:25][CH:26]=1>C1COCC1>[C:1]([O:5][C:6](=[O:13])[NH:7][CH:8]1[CH2:11][CH:10]([O:12][C:22]2[C:21]([Br:20])=[CH:26][N:25]=[C:24]([Cl:27])[N:23]=2)[CH2:9]1)([CH3:4])([CH3:2])[CH3:3]

参加物

5

実験手順

To a solution of (3-hydroxy-cyclobutyl)-carbamic acid tert-butyl ester (2.5 g, 13.3 mmol) in THF (40 mL) were added Cs2CO3 (8.6 g, 26.6 mmol) and 5-bromo-2,4-dichloro-pyrimidine (3 g, 13.3 mmol). The reaction mixture was heated at reflux overnight. The reaction mixture was filtered and concentrated, diluted with EtOAc and water. The aqueous phase was extracted with EtOAc (3×100 mL) and the combined organic extracts were washed with brine (60 mL), dried over MgSO4, filtered, and concentrated. Purification by flash column chromatography on silica gel to give the product (4.75 g, 12.6 mmol, yield: 95%). ESI-MS (M+1): 378 calc. for C13H17BrClN3O3 377.

後処理

  1. temperatureThe reaction mixture was heated
  2. temperatureat reflux overnight
  3. filtrationThe reaction mixture was filtered
  4. concentrationconcentrated
  5. additiondiluted with EtOAc and water
  6. extractionThe aqueous phase was extracted with EtOAc (3×100 mL)
  7. washthe combined organic extracts were washed with brine (60 mL)
  8. dry with materialdried over MgSO4
  9. filtrationfiltered
  10. concentrationconcentrated
  11. customPurification by flash column chromatography on silica gel

出典と根拠

ORDレコード
ord-a83f18f38fec4b1aad37f75dce3412a0
出典データセット
uspto-grants-2015_02
特許番号
US08952037B2

反応ノート

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