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Methylamine → 2-Chloro-N-methyl-5-(trifluoromethyl)pyrimidin-4-amine

HRID 1503296
ノート
印刷プレビュー

反応式

HRID 1503296 の反応式
[Cl:1][C:2]1[N:7]=[C:6](Cl)[C:5]([C:9]([F:12])([F:11])[F:10])=[CH:4][N:3]=1.[CH2:13]([N:15](CC)CC)C.CN>CO>[Cl:1][C:2]1[N:7]=[C:6]([NH:15][CH3:13])[C:5]([C:9]([F:12])([F:11])[F:10])=[CH:4][N:3]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 6329MethylamineHCID 8471TriethylamineHCID 27827742,4-Dichloro-5-(trifluoromethyl)pyrimidine

生成物 1

HCID 210775872-Chloro-N-methyl-5-(trifluoromethyl)pyrimidin-4-amine収率 45.7%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒2 回

実験手順

To a cooled (−10° C.) solution of 2,4-dichloro-5-trifluoromethylpyrimidine (20 g, 0.089 mol) in methanol (100 mL) was added triethylamine (12.5 mL, 0.089 mol) and a 2 M solution of methylamine in methanol (45 mL). The reaction was allowed to warm to room temperature and stirred overnight. The reaction was then concentrated and re-dissolved in ethyl acetate. The solution was washed with sat. NaHCO3, brine, dried over MgSO4, filtered and concentrated. The crude product was purified by column chromatography (5-25% EtOAc in heptane) to give 2-chloro-N-methyl-5-(trifluoromethyl)pyrimidin-4-amine (8.6 g, 45%). 1H-NMR (DMSO): δ 8.37 (s, 1H), 7.90 (s, 1H), 2.90 (s, 3H).

後処理

  1. concentrationThe reaction was then concentrated
  2. dissolutionre-dissolved in ethyl acetate
  3. washThe solution was washed with sat. NaHCO3, brine
  4. dry with materialdried over MgSO4
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customThe crude product was purified by column chromatography (5-25% EtOAc in heptane)

出典と根拠

ORDレコード
ord-7d3d3f6357a54b83bf55dccdb3b08bb4
出典データセット
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09212173B2

反応ノート

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