4-Chloro-6-hydrazinylpyrimidine → 2-(6-Chloropyrimidin-4-yl)-4-pyridin-3-yl-1,2-dihydro-3H-pyrazol-3-one

HRID 37898

反応式

HRID 37898 の反応式
[Cl:1][C:2]1[CH:7]=[C:6]([NH:8][NH2:9])[N:5]=[CH:4][N:3]=1.CN(C)[CH:12]=[C:13]([C:19]1[CH:20]=[N:21][CH:22]=[CH:23][CH:24]=1)[C:14](OCC)=[O:15]>C(O)(=O)C>[Cl:1][C:2]1[N:3]=[CH:4][N:5]=[C:6]([N:8]2[C:14](=[O:15])[C:13]([C:19]3[CH:20]=[N:21][CH:22]=[CH:23][CH:24]=3)=[CH:12][NH:9]2)[CH:7]=1

参加物

4

実験手順

At RT, 30.0 g (207.5 mmol) of the compound from Example 7A and 50.3 g (228.3 mmol) of the compound from Example 3A are stirred in 1000 ml of glacial acetic acid for 16 h. For work-up, the solvent is removed on a rotary evaporator, the residue is taken up in ethyl acetate and washed with saturated sodium bicarbonate solution until neutral, and the organic phase is concentrated under reduced pressure. The residue is dissolved in 1000 ml of ethanol, 42.8 ml (41.1 g, 228.3 mmol) of 30% strength methanolic sodium methoxide solution are added and the mixture is stirred at RT for 2 h. The reaction mixture is then adjusted to pH 5 using 1 N hydrochloric acid and stirred for 16 h. The precipitate is filtered off, the filter residue is washed with water and ethanol and the product is dried under reduced pressure.

後処理

  1. customFor work-up, the solvent is removed on a rotary evaporator
  2. washwashed with saturated sodium bicarbonate solution until neutral, and the organic phase
  3. concentrationis concentrated under reduced pressure
  4. dissolutionThe residue is dissolved in 1000 ml of ethanol
  5. addition42.8 ml (41.1 g, 228.3 mmol) of 30% strength methanolic sodium methoxide solution are added
  6. stirringstirred for 16 h
  7. filtrationThe precipitate is filtered off
  8. washthe filter residue is washed with water and ethanol
  9. customthe product is dried under reduced pressure

出典と根拠

ORDレコード
ord-2693a4b649f643509bbdb14e7cf82ccb
出典データセット
uspto-grants-2013_09
特許番号
US08524699B2

関連ノート

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