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Methanol → 4,6-Dimethoxy-2-methylpyrimidin-5-amine

HRID 1398864
ノート
印刷プレビュー

反応式

HRID 1398864 の反応式
[CH3:1][O-:2].[Na+].Cl[C:5]1[C:10]([NH2:11])=[C:9](Cl)[N:8]=[C:7]([CH3:13])[N:6]=1.[CH3:14][OH:15]>>[CH3:1][O:2][C:5]1[C:10]([NH2:11])=[C:9]([O:15][CH3:14])[N:8]=[C:7]([CH3:13])[N:6]=1
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

4

反応物 3

HCID 887MethanolHCID 7366744,6-Dichloro-2-methylpyrimidin-5-amineHCID 10942334Sodium Methoxide

生成物 1

HCID 212392004,6-Dimethoxy-2-methylpyrimidin-5-amine収率 100%

反応条件

温度
70 °C

実験手順

Sodium methoxide (28% solution in methanol, 150 mL) was added dropwise to a stirred solution of 4,6-dichloro-2-methylpyrimidin-5-amine (15.0 g, 84.3 mmol) in methanol (150 mL) at 0° C., and the mixture was stirred at room temperature for 1 hr, at 70° C. for 6 hr. The mixture was concentrated, diluted with aqueous saturated ammonium chloride and extracted with ethyl acetate. The combined organic layer was washed with brine, dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo to give the title compound as a yellow solid (14.2 g, 84.3 mmol, 100%).

後処理

  1. concentrationThe mixture was concentrated
  2. additiondiluted with aqueous saturated ammonium chloride
  3. extractionextracted with ethyl acetate
  4. washThe combined organic layer was washed with brine
  5. dry with materialdried over anhydrous magnesium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-5d3c793f3772441ab236261921ef7f75
出典データセット
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08901141B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート