Hydrochloric Acid → HCID 23446892、化合物

HRID 1841631ノート

反応式

HRID 1841631 の反応式
Cl.[NH2:2][C:3]1[C:11]([Cl:12])=[CH:10][CH:9]=[C:8]([CH3:13])[C:4]=1[C:5]([NH2:7])=O>C(OCC)C.ClCCCl>[NH2:2][C:3]1[C:11]([Cl:12])=[CH:10][CH:9]=[C:8]([CH3:13])[C:4]=1[C:5]#[N:7]

参加物

5

反応条件

温度
120 °C

実験手順

1.18 g (0.033 mol) of hydrogen chloride, dissolved in 35 ml of diethyl ether, were added at 22 to 30° C. with stirring to a suspension of 5 g (0.027 mol) of the compound from example 3 in 50 ml of 1,2-dichloroethane and the mixture was then concentrated in vacuo. The residue was treated with 150 ml of phosphorus oxychloride and the mixture was stirred at 120° C. for 3 h. The reaction mixture was then concentrated in vacuo, the residue was dissolved in methylene chloride, and the solution was treated with water and neutralized using 2 N sodium hydroxide solution. After the phase separation, the organic phase was again washed with water, then with saturated sodium chloride solution, and dried over magnesium sulfate. After concentration, 2.4 g (48% of theory) of the title compound were obtained as a yellowish powder of m.p. 77-80° C.

後処理

  1. additionwere added at 22 to 30° C.
  2. concentrationthe mixture was then concentrated in vacuo
  3. additionThe residue was treated with 150 ml of phosphorus oxychloride
  4. concentrationThe reaction mixture was then concentrated in vacuo
  5. dissolutionthe residue was dissolved in methylene chloride
  6. additionthe solution was treated with water
  7. customAfter the phase separation
  8. washthe organic phase was again washed with water
  9. dry with materialwith saturated sodium chloride solution, and dried over magnesium sulfate
  10. concentrationAfter concentration, 2.4 g (48% of theory) of the title compound
  11. customwere obtained as a yellowish powder of m.p. 77-80° C.

出典と根拠

ORDレコード
ord-8479d47b6bc3457cbc42a520fb41b705
出典データセット
uspto-grants-2004_01
特許番号
US06683213B1

反応ノート

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