Acetic Acid → 7-Benzyl-3-butylxanthine

HRID 2234962

反応式

HRID 2234962 の反応式
[CH2:1]([N:8]1[C:16]2[C:15](=[O:17])[NH:14][C:13](=[O:18])[NH:12][C:11]=2[N:10]=[CH:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(=O)([O-])[O-].[K+].[K+].[CH2:25](I)[CH2:26][CH2:27][CH3:28].C(O)(=O)C>CN(C=O)C>[CH2:25]([N:12]1[C:11]2[N:10]=[CH:9][N:8]([CH2:1][C:2]3[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=3)[C:16]=2[C:15](=[O:17])[NH:14][C:13]1=[O:18])[CH2:26][CH2:27][CH3:28]

参加物

6

反応物 4

HCID 176Acetic AcidHCID 10962Butyl iodideHCID 11430Potassium CarbonateHCID 125005077-Benzyl-1H-purine-2,6(3H,7H)-dione

生成物 1

HCID 39938667-Benzyl-3-butylxanthine収率 45%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

7-benzyl-3,7-dihydro-1H-purine-2,6-dione (17.14 g, 70.8 mmol) [Synthetic Communications, 20(16), 2459-2467, 1990] and potassium carbonate (11.43 g, 82.8 mmol) were suspended in DMF (400 mL) at 40° C. After stirring for thirty minutes, butyl iodide (8.76 mL, 77.0 mmol) was added, and the mixture was stirred at 40° C. overnight. 50% Aqueous acetic acid (60 mL) was added, and the solution was concentrated under reduced pressure. The residue was suspended in water (500 mL), and the products were extracted into chloroform. The organics were collected, concentrated, and product was isolated using flash chromatography eluting with 1% methanol in dichloromethane to provide the product (9.49 g, 45%); 1H NMR (400 MHz; CDCl3) δ: 0.95 (3H, t), 1.34-1.41 (2H, m), 1.70-1.78 (2H, m), 4.05 (2H, t), 5.46 (2H, s), 7.31-7.40 (5H, m), 7.56 (1H, s), 8.21 (1H, br.s); m/z 299[MH+].

後処理

  1. stirringthe mixture was stirred at 40° C. overnight
  2. concentrationthe solution was concentrated under reduced pressure
  3. extractionthe products were extracted into chloroform
  4. customThe organics were collected
  5. concentrationconcentrated
  6. customproduct was isolated
  7. washeluting with 1% methanol in dichloromethane

出典と根拠

ORDレコード
ord-c60e62b786e647abb187e6629f772184
出典データセット
uspto-grants-2010_05
特許番号
US07713982B2

関連ノート

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