Water → 4-(2-Difluoromethoxypyridin-4-Yloxy)-2-(Pyrazin-2-yl)-Pyrimidine

HRID 651733

反応式

HRID 651733 の反応式
O.Cl[C:3](Cl)(Cl)[CH2:4][CH:5](Cl)OCC.Cl.[N:13]1[CH:18]=[CH:17][N:16]=[CH:15][C:14]=1[C:19]([NH2:21])=[NH:20].[F:22][CH:23]([F:32])[O:24][C:25]1[CH:30]=[C:29]([OH:31])[CH:28]=[CH:27][N:26]=1.C(=O)([O-])[O-].[K+].[K+].ClC(Cl)=CC=O>C(COC)OC.Cl.N1C=CN=CC=1C(N)=N>[F:32][CH:23]([F:22])[O:24][C:25]1[CH:30]=[C:29]([O:31][C:3]2[CH:4]=[CH:5][N:21]=[C:19]([C:14]3[CH:15]=[N:16][CH:17]=[CH:18][N:13]=3)[N:20]=2)[CH:28]=[CH:27][N:26]=1

参加物

9

反応条件

温度
60 °C

実験手順

Water (20 mmoles) is added to a solution of 1,1,1,3-tetrachloro-3-ethoxypropane (10 mmoles) in dimethoxyethane (25 ml). The mixture is stirred for 2 h at 60° C. The resulting mixture is slowly added to a mixture consisting of a pyrazine-2-carboxamidine hydrochloride (10 mmoles), 2-difluoromethoxypyridin-4-ol (10 mmoles), potassium carbonate (60 mmoles) and dimethoxyethane (50 ml), which is stirred under reflux. When the addition of 3,3-dichloroacrolein solution is completed additional pyrazine-2-carboxamidine hydrochloride (0.5 mmoles) is added. The reaction mixture is stirred for 2 hours under reflux and subsequently cooled down to ambient temperature, filtered through silica, and the organic phase is concentrated in vacuo. The residue is purified by chromatography on SiO2 (ethyl acetate) to yield 2,60 g (82%) of beige crystals having a melting point of 128-129° C.

後処理

  1. additionThe resulting mixture is slowly added to a mixture
  2. stirringis stirred
  3. temperatureunder reflux
  4. additionis added
  5. stirringThe reaction mixture is stirred for 2 hours
  6. temperatureunder reflux
  7. temperaturesubsequently cooled down to ambient temperature
  8. filtrationfiltered through silica
  9. concentrationthe organic phase is concentrated in vacuo
  10. customThe residue is purified by chromatography on SiO2 (ethyl acetate)

出典と根拠

ORDレコード
ord-6a574ee6dba64ceaabfc039473b65c06
出典データセット
uspto-grants-2001_08
特許番号
US06281358B1

関連ノート

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