3-Ethoxy-2-propenoyl chloride → 1,6,7,8,9,10-Hexahydro-2h-azepino[3,2-g]quinolin-2-one

HRID 459711

反応式

HRID 459711 の反応式
[NH:1]1[C:7]2[CH:8]=[C:9]([NH2:12])[CH:10]=[CH:11][C:6]=2[CH2:5][CH2:4][CH2:3][CH2:2]1.C([O:15][CH:16]=[CH:17][C:18](Cl)=O)C>C(Cl)Cl.[OH-].[Na+]>[NH:12]1[C:9]2[C:10](=[CH:11][C:6]3[CH2:5][CH2:4][CH2:3][CH2:2][NH:1][C:7]=3[CH:8]=2)[CH:18]=[CH:17][C:16]1=[O:15]

参加物

5

反応条件

温度
50 °C

実験手順

A solution of 2,3,4,5-tetrahydro-1H-1-benzazapin-8-amine (0.6 g, 3.4 mmol) and 3-ethoxyacryloyl chloride (0.45 g, 3.4 mmol) in CH2Cl2 (50 mL) and 3N NaOH (10 mL) was stirred for 1 h at ambient temperature. The reaction was partitioned between CH2Cl2 and water. The organic layer was concentrated and the remaining brown oil was dissolved in 70% aq. H2SO4 (20 mL) and heated gently (50° C.) for 2 h. The reaction was cooled and neutralized with aq. NH4OH and partitioned between water and EtOAc. The organic layer was washed with brine, dried over MgSO4, filtered and concentrated. The residue was dissolved in DMF (1 mL) and purified on a GILSON automated system affixed with a YMC COMBIFLASH 50 mm×20 mm reverse phase column eluted 5–95% CH3CN in water at 30 mL/min over 10.5 min to provide pure desired product. HRMS m/z (M+1) calcd 215.1179; found 215.1186.

後処理

  1. customThe reaction was partitioned between CH2Cl2 and water
  2. concentrationThe organic layer was concentrated
  3. dissolutionthe remaining brown oil was dissolved in 70% aq. H2SO4 (20 mL)
  4. temperatureThe reaction was cooled
  5. custompartitioned between water and EtOAc
  6. washThe organic layer was washed with brine
  7. dry with materialdried over MgSO4
  8. filtrationfiltered
  9. concentrationconcentrated
  10. dissolutionThe residue was dissolved in DMF (1 mL)
  11. custompurified on a GILSON automated system
  12. washeluted 5–95% CH3CN in water at 30 mL/min over 10.5 min

出典と根拠

ORDレコード
ord-f67beddc9b33443db36a36f7388ba7e4
出典データセット
uspto-grants-2007_03
特許番号
US07196076B2

関連ノート

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