tert-Butyl bromoacetate → t-Butyl (5-nitro-1-methyl-uracilyl)acetate

HRID 2257117

反応式

HRID 2257117 の反応式
[N+:1]([C:4]1[C:5](=[O:12])[NH:6][C:7](=[O:11])[N:8]([CH3:10])[CH:9]=1)([O-:3])=[O:2].Br[CH2:14][C:15]([O:17][C:18]([CH3:21])([CH3:20])[CH3:19])=[O:16]>O>[C:18]([O:17][C:15](=[O:16])[CH2:14][N:6]1[C:5](=[O:12])[C:4]([N+:1]([O-:3])=[O:2])=[CH:9][N:8]([CH3:10])[C:7]1=[O:11])([CH3:21])([CH3:20])[CH3:19]

参加物

4

反応物 2

HCID 79177tert-Butyl bromoacetateHCID 27557345-Nitro-1-methyl-uracil

生成物 1

HCID 53829665t-Butyl (5-nitro-1-methyl-uracilyl)acetate収率 59%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

Sodium hydride (0.51 g of a 60% dispersion in mineral oil, 13 mmol) was washed with pentane three times (4 mL each). The compound of Example 109 (2.00 g, 12 mmole) was added portionwise. After the addition was complete, the reaction mixture was stirred for 30 minutes under a nitrogen atmosphere. t-Butyl bromoacetate (1.73 g, 12 mmole) was added in one portion, and the solution was stirred for 3 hours. The reaction mixture was diluted with water (200 mL), and extracted with ethyl acetate (3×50 mL). The combined organic extracts were washed with water (3×50 mL), then brine, dried over magnesium sulfate. The solvent was concentrated, hexanes were added and the solvent was removed in vacuo to afford the title compound (1.97 g) in 59% yield. Rf=0.38 (silica gel, 20% ethyl acetate in dichloromethane.

後処理

  1. washSodium hydride (0.51 g of a 60% dispersion in mineral oil, 13 mmol) was washed with pentane three times (4 mL each)
  2. additionAfter the addition
  3. stirringthe solution was stirred for 3 hours
  4. extractionextracted with ethyl acetate (3×50 mL)
  5. washThe combined organic extracts were washed with water (3×50 mL)
  6. dry with materialbrine, dried over magnesium sulfate
  7. concentrationThe solvent was concentrated
  8. additionhexanes were added
  9. customthe solvent was removed in vacuo

出典と根拠

ORDレコード
ord-b117741c08764cec9dfd9a311338c8a8
出典データセット
uspto-grants-1997_08
特許番号
US05656645

関連ノート

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