Cesium carbonate → Tert-butyl 4-(4-methoxycarbonylphenyl)-1,4-diazepane-1-carboxylate

HRID 16760

反応式

HRID 16760 の反応式
I[C:2]1[CH:11]=[CH:10][C:5]([C:6]([O:8][CH3:9])=[O:7])=[CH:4][CH:3]=1.[N:12]1([C:19]([O:21][C:22]([CH3:25])([CH3:24])[CH3:23])=[O:20])[CH2:18][CH2:17][CH2:16][NH:15][CH2:14][CH2:13]1.C(=O)([O-])[O-].[Cs+].[Cs+].C(C1CCCCC1=O)(=O)C>CN(C=O)C.[Cu](I)I>[CH3:9][O:8][C:6]([C:5]1[CH:10]=[CH:11][C:2]([N:15]2[CH2:16][CH2:17][CH2:18][N:12]([C:19]([O:21][C:22]([CH3:25])([CH3:24])[CH3:23])=[O:20])[CH2:13][CH2:14]2)=[CH:3][CH:4]=1)=[O:7]

参加物

7

反応物 4

HCID 10796Cesium carbonateHCID 134002-AcetylcyclohexanoneHCID 69273Methyl 4-iodobenzoateHCID 2756058Tert-butyl 1,4-diazepane-1-carboxylate

生成物 1

HCID 57362684Tert-butyl 4-(4-methoxycarbonylphenyl)-1,4-diazepane-1-carboxylate収率 13.2%

試薬・触媒・溶媒 2

HCID 83717Copper iodide触媒HCID 6228Dimethylformamide溶媒

反応条件

温度
90 °C

実験手順

Methyl 4-iodobenzoate (1.00 g, 3.82 mmol, 1.0 eq) was dissolved in DMF and tert-butyl 1,4-diazepane-1-carboxylate (765 mg, 3.82 mmol, 1.0 eq), caesium carbonate (2.49 g, 7.63 mmol, 2.0 eq), 2-acetylcyclohexanone (101 μl, 0.76 mmol, 0.20 eq [20 mol %]) and copper iodide (37 mg, 0.19 mmol, 0.05 eq [5 mol %]) were added. The reaction mixture was stirred at 90° C. under nitrogen for 7 h. The reaction mixture was evaporated, dissolved in DCM (50 ml), washed with water (20 ml), saturated ammonium chloride solution (20 ml), dried over MgSO4, filtered and evaporated. The crude product was purified by silica column chromatography, eluting with 0-1% MeOH in DCM. The product containing fractions were combined, evaporated and dried in vacuo to give tert-butyl 4-(4-methoxycarbonylphenyl)-1,4-diazepane-1-carboxylate (168 mg, 13%) as a yellow oil.

後処理

  1. customThe reaction mixture was evaporated
  2. dissolutiondissolved in DCM (50 ml)
  3. washwashed with water (20 ml), saturated ammonium chloride solution (20 ml)
  4. dry with materialdried over MgSO4
  5. filtrationfiltered
  6. customevaporated
  7. customThe crude product was purified by silica column chromatography
  8. washeluting with 0-1% MeOH in DCM
  9. additionThe product containing fractions
  10. customevaporated
  11. customdried in vacuo

出典と根拠

ORDレコード
ord-bf580b2f31564622a5397ead6f2f9ef0
出典データセット
uspto-grants-2010_06
特許番号
US07737149B2

関連ノート

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