Potassium Iodide → 6-Chloro-1-butyl-3-propyluracil

HRID 746254ノート

反応式

HRID 746254 の反応式
[Cl:1][C:2]1[NH:7][C:6](=[O:8])[N:5]([CH2:9][CH2:10][CH3:11])[C:4](=[O:12])[CH:3]=1.[CH2:13](Br)[CH2:14][CH2:15][CH3:16].C(=O)([O-])[O-].[K+].[K+].[I-].[K+]>CN(C)C=O>[Cl:1][C:2]1[N:7]([CH2:13][CH2:14][CH2:15][CH3:16])[C:6](=[O:8])[N:5]([CH2:9][CH2:10][CH3:11])[C:4](=[O:12])[CH:3]=1

参加物

6

実験手順

A mixture of 7 g of 6-chloro-3-propyluracil, 10.28 g of butyl bromide, 10.28 g of potassium carbonate, 6 g of potassium iodide and 80 ml of dimethylformamide was stirred at room temperature for 23 hours. After the reaction solution was concentrated to dryness under reduced pressure, 300 ml each of chloroform and water were added to the residue, and the mixture was shaken. The chloroform layer was washed with water and then concentrated to dryness under reduced pressure to give 6-chloro-1-butyl-3-propyluracil as a brown oily substance. This product, without being purified, was dissolved in 20 ml of ethanol, and 20 ml of 100% hydrazine hydrate was added to the solution, followed by stirring at room temperature for 1 hour. The reaction solution was concentrated to dryness under reduced pressure and the residue was washed with water and recrystallized from a mixture of ethanol, ethyl acetate and isopropyl ether to give 7 g of yellow prisms of 6-hydrazino-1-butyl-3-propyluracil melting at 146°-147° C.

後処理

  1. concentrationAfter the reaction solution was concentrated to dryness under reduced pressure, 300 ml each of chloroform and water
  2. additionwere added to the residue
  3. stirringthe mixture was shaken
  4. washThe chloroform layer was washed with water
  5. concentrationconcentrated to dryness under reduced pressure

出典と根拠

ORDレコード
ord-2b00b6cd262b48e9853abae1963e8b52
出典データセット
uspto-grants-1986_07
特許番号
US04603203

反応ノート

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