Stannous chloride dihydrate → 4,6-Dichloro-2-(methylsulfanyl)pyrimidin-5-amine

HRID 2063510

反応式

HRID 2063510 の反応式
[Cl:1][C:2]1[C:7]([N+:8]([O-])=O)=[C:6]([Cl:11])[N:5]=[C:4]([S:12][CH3:13])[N:3]=1.O.O.Cl[Sn]Cl>CCO>[Cl:1][C:2]1[C:7]([NH2:8])=[C:6]([Cl:11])[N:5]=[C:4]([S:12][CH3:13])[N:3]=1

参加物

4

反応条件

温度
90 °C

実験手順

To a solution of 4,6-dichloro-2-methylsulfanyl-5-nitro-pyrimidine (1.0 g, 4.2 mmol) in EtOH (20 mL) was added SnCl2.2H2O (3.8 g, 17 mmol). The mixture was heated to 90° C. After 2 h, the reaction mixture was cooled and the solution was concentrated. The residue was treated with saturated (satd.) aqueous (aq.) NaHCO3 until pH 8. The resulting mixture was then extracted with EtOAc (3×100 mL). The combined organic extracts were dried, filtered, and concentrated. The residue was purified by FCC to afford a colorless solid (723 mg, 87%). MS (ESI): mass calcd. for C5H5Cl2N3S, 208.9; m/z found, 210.3 [M+H]+. 1H NMR ((CD3)2SO): 5.89 (s, 2H), 2.45 (s, 3H).

後処理

  1. temperaturethe reaction mixture was cooled
  2. concentrationthe solution was concentrated
  3. additionThe residue was treated with saturated (satd.) aqueous (aq.) NaHCO3 until pH 8
  4. extractionThe resulting mixture was then extracted with EtOAc (3×100 mL)
  5. customThe combined organic extracts were dried
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customThe residue was purified by FCC

出典と根拠

ORDレコード
ord-47f76b07c5db4b88864b8a55655db630
出典データセット
uspto-grants-2012_10
特許番号
US08288397B2

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