Potassium Carbonate → 4-(2-Butynyloxy)-6-(3-trifluoromethylpiperidino)pyrimidine

HRID 2069891ノート

反応式

HRID 2069891 の反応式
F[C:2]1[CH:7]=[C:6](F)[N:5]=[CH:4][N:3]=1.[C:9](=O)([O-])[O-].[K+].[K+].[CH2:15]([OH:19])[C:16]#[C:17][CH3:18].[F:20][C:21]([F:28])([F:27])[CH:22]1[CH2:26][CH2:25][NH:24][CH2:23]1>O.C1(C)C=CC=CC=1.C(N(CC)CC)C>[CH2:15]([O:19][C:2]1[CH:7]=[C:6]([N:24]2[CH2:25][CH2:9][CH2:26][CH:22]([C:21]([F:20])([F:27])[F:28])[CH2:23]2)[N:5]=[CH:4][N:3]=1)[C:16]#[C:17][CH3:18]

参加物

8

反応条件

温度
30 °C

実験手順

To a mixture obtained by adding 110.0 g of 4,6-difluoropyrimidine, 132.3 g of potassium carbonate and 19.2 g of triethylamine to 220.0 g of toluene, 69.8 g of 2-butyn-1-ol is added dropwise at 25 to 30° C. over one hour, followed by stirring at 30° C. Then, 220.0 g of water is added dropwise into the reaction mixture, followed by stirring. Then, 152.4 g of 3-trifluoromethylpyrrolidine is added dropwise and, after the mixture is stirred at 30° C., the reaction mixture is allowed to stand. After separating into the organic layer and the aqueous layer, the aqueous layer is removed and the organic layer is washed once with 220.0 g of 5% hydrochloric acid and then washed once with 220.0 g of water. The organic layer is concentrated to obtain 4-(2-butynyloxy)-6-(3-trifluoromethylpiperidino)pyrimidine (hereinafter referred to as the present compound (2)).

後処理

  1. customTo a mixture obtained
  2. additionis added dropwise at 25 to 30° C. over one hour
  3. stirringby stirring
  4. stirringafter the mixture is stirred at 30° C.
  5. customAfter separating into the organic layer
  6. customthe aqueous layer, the aqueous layer is removed
  7. washthe organic layer is washed once with 220.0 g of 5% hydrochloric acid
  8. washwashed once with 220.0 g of water
  9. concentrationThe organic layer is concentrated

出典と根拠

ORDレコード
ord-7e674331cfe14eaaafee9cbb79f9b92b
出典データセット
uspto-grants-2012_10
特許番号
US08299245B2

反応ノート

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