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Dihydrouracil → 1-{4-[7-propyl-3-(trifluoromethyl)-1,2-benzisoxazol-6-yl]butyl}dihydropyrimidine-2,4(1H,3H)-dione

HRID 1245341
ノート
印刷プレビュー

反応式

HRID 1245341 の反応式
CS(O[CH2:6][CH2:7][CH2:8][CH2:9][C:10]1[CH:22]=[CH:21][C:13]2[C:14]([C:17]([F:20])([F:19])[F:18])=[N:15][O:16][C:12]=2[C:11]=1[CH2:23][CH2:24][CH3:25])(=O)=O.C([O-])([O-])=O.[Cs+].[Cs+].[NH:32]1[CH2:39][CH2:38][C:36](=[O:37])[NH:35][C:33]1=[O:34]>CN(C=O)C>[CH2:23]([C:11]1[C:12]2[O:16][N:15]=[C:14]([C:17]([F:20])([F:19])[F:18])[C:13]=2[CH:21]=[CH:22][C:10]=1[CH2:9][CH2:8][CH2:7][CH2:6][N:32]1[CH2:39][CH2:38][C:36](=[O:37])[NH:35][C:33]1=[O:34])[CH2:24][CH3:25]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 649DihydrouracilHCID 10796Cesium carbonateHCID 219109934-[7-Propyl-3-(trifluoromethyl)-1,2-benzisoxazol-6-yl]butyl methanesulfonate

生成物 1

HCID 219110301-{4-[7-propyl-3-(trifluoromethyl)-1,2-benzisoxazol-6-yl]butyl}dihydropyrimidine-2,4(1H,3H)-dione

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

A mixture of 4-[7-propyl-3-(trifluoromethyl)-1,2-benzisoxazol-6-yl]butyl methanesulfonate (60 mg, 0.16 mmol), from this Example step 5, Cs2CO3 (206 mg, 0.63 mmol) and 5,6-dihydrouracil (54.2 mg, 0.48 mmol) in dry DMF (1.5 mL) was stirred at room temperature overnight. The reaction mixture was partitioned between ethyl acetate and water. Combined organic extracts were washed with water and brine, dried over Na2SO4 and the solvent evaporated in vacuo. The residue was purified by preparative TLC using ethyl acetate to give the title compound.

後処理

  1. customwas stirred at room temperature overnight
  2. customThe reaction mixture was partitioned between ethyl acetate and water
  3. washCombined organic extracts were washed with water and brine
  4. dry with materialdried over Na2SO4
  5. customthe solvent evaporated in vacuo
  6. customThe residue was purified by preparative TLC

出典と根拠

ORDレコード
ord-7ddbc9cd13e045ecbe211289e43f59e9
出典データセット
uspto-grants-2006_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07125865B2

反応ノート

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