1-Bromo-3-chloropropane → 3-benzyl-6-chloro-1-(3-chloropropyl)-5-isopropylpyrimidine-2,4(1H,3H)-dione

HRID 357123

反応式

HRID 357123 の反応式
[CH2:1]([N:8]1[C:13](=[O:14])[C:12]([CH:15]([CH3:17])[CH3:16])=[C:11]([Cl:18])[NH:10][C:9]1=[O:19])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(=O)([O-])[O-].[K+].[K+].Br[CH2:27][CH2:28][CH2:29][Cl:30]>CN(C)C=O>[CH2:1]([N:8]1[C:13](=[O:14])[C:12]([CH:15]([CH3:16])[CH3:17])=[C:11]([Cl:18])[N:10]([CH2:27][CH2:28][CH2:29][Cl:30])[C:9]1=[O:19])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

参加物

5

反応条件

温度
90 °C

実験手順

To a suspension of 20.91 g (75 mmol) of 3-benzyl-6-chloro-5-isopropylpyrimidine-2,4(1H,3H)-dione and 16.58 g (120 mmol) of potassium carbonate in 120 ml of N,N-dimethylformamide, 14.8 ml (150 mmol) of 1-bromo-3-chloropropane was added at room temperature. This mixture was stirred at 90° C. for 2 hours. After cooling, the reaction mixture was concentrated to dryness; the resulting residue was dissolved in chloroform-water. After the organic layer was washed with water and dried, the solvent was distilled off to yield an oily substance, which was then purified by column chromatography (eluent, n-hexane/ethyl acetate=5/1→3/1) to yield 8.06 g (30.1%, yellow oily substance) of the desired product.

後処理

  1. additionwas added at room temperature
  2. temperatureAfter cooling
  3. concentrationthe reaction mixture was concentrated to dryness
  4. dissolutionthe resulting residue was dissolved in chloroform-water
  5. washAfter the organic layer was washed with water
  6. customdried
  7. distillationthe solvent was distilled off
  8. customto yield an oily substance, which
  9. customwas then purified by column chromatography (eluent, n-hexane/ethyl acetate=5/1→3/1)

出典と根拠

ORDレコード
ord-80e57133d85b4699a4f6e2b9ff3fc23c
出典データセット
uspto-grants-1998_11
特許番号
US05840732

関連ノート

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