Cesium carbonate → Dimethyl 4-benzyloxy-1-(3-bromopropyl)-1H-pyrazole-3,5-dicarboxylate

HRID 1453865

反応式

HRID 1453865 の反応式
[CH2:1]([O:8][C:9]1[C:10]([C:18]([O:20][CH3:21])=[O:19])=[N:11][NH:12][C:13]=1[C:14]([O:16][CH3:17])=[O:15])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Br[C:23]([Br:26])([CH3:25])C.[C:27]([O-])([O-])=O.[Cs+].[Cs+]>CN(C=O)C>[CH2:1]([O:8][C:9]1[C:13]([C:14]([O:16][CH3:17])=[O:15])=[N:12][N:11]([CH2:27][CH2:25][CH2:23][Br:26])[C:10]=1[C:18]([O:20][CH3:21])=[O:19])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

参加物

5

反応物 3

HCID 10796Cesium carbonateHCID 116582,2-DibromopropaneHCID 57528491dimethyl 4-benzyloxy-1H-pyrazole-3,5-dicarboxylate

生成物 1

HCID 69080907Dimethyl 4-benzyloxy-1-(3-bromopropyl)-1H-pyrazole-3,5-dicarboxylate

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

To a solution of dimethyl 4-benzyloxy-1H-pyrazole-3,5-dicarboxylate (200 mg, 0.689 mmol) in DMF (3 mL) under an atmosphere of nitrogen at 0° C. was added dibromopropane (211 μL, 2.067 mmol) and Cs2CO3 (269 mg, 0.827 mmol). The ice bath was removed, and the reaction was stirred at room temperature overnight. The solvent was removed in vacuo, and the resulting residue was partitioned between EtOAc and water. The aqueous layer was extracted into EtOAc once, and the combined organic extracts were washed with brine, dried over Na2SO4, and concentrated in vacuo. the residue was purified by flash column chromatography on silica gel using a 0-50% EtOAc/hexanes gradient elution. Collection and concentration of the appropriate fractions afforded the compound. 1H NMR (400 MHz, CDCl3) δ 7.47-7.44 (m, 2H), 7.40-7.34 (m, 3M), 5.13 (s, 2H), 4.71-4.67 (t, 2H), 3.96 (s, 3H), 3.87 (s, 3H), 3.39-3.36 (t, 2H), 2.45-2.38 (dt, 2H); ES MS (M+1)=412.

後処理

  1. customThe ice bath was removed
  2. customThe solvent was removed in vacuo
  3. customthe resulting residue was partitioned between EtOAc and water
  4. extractionThe aqueous layer was extracted into EtOAc once
  5. washthe combined organic extracts were washed with brine
  6. dry with materialdried over Na2SO4
  7. concentrationconcentrated in vacuo
  8. customthe residue was purified by flash column chromatography on silica gel using
  9. washa 0-50% EtOAc/hexanes gradient elution
  10. customCollection and concentration of the appropriate fractions
  11. customafforded the compound

出典と根拠

ORDレコード
ord-23e4a8f716d14da49f8053f2daa917f6
出典データセット
uspto-grants-2009_01
特許番号
US07476666B2

関連ノート

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