Potassium Iodide → 3-Cyclobutyl-7-(2,4-difluoro-benzyloxy)-2,3,4,5-tetrahydro-1H-benzo[d]azepine

HRID 641483노트

반응식

HRID 641483 반응식
C(=O)([O-])[O-].[K+].[K+].[CH:7]1([N:11]2[CH2:17][CH2:16][C:15]3[CH:18]=[C:19]([OH:22])[CH:20]=[CH:21][C:14]=3[CH2:13][CH2:12]2)[CH2:10][CH2:9][CH2:8]1.[F:23][C:24]1[CH:31]=[C:30]([F:32])[CH:29]=[CH:28][C:25]=1[CH2:26]Br.[I-].[K+]>CC(=O)CC>[CH:7]1([N:11]2[CH2:17][CH2:16][C:15]3[CH:18]=[C:19]([O:22][CH2:26][C:25]4[CH:28]=[CH:29][C:30]([F:32])=[CH:31][C:24]=4[F:23])[CH:20]=[CH:21][C:14]=3[CH2:13][CH2:12]2)[CH2:10][CH2:9][CH2:8]1

참가 물질

6

실험 절차

Potassium carbonate (778 mg, 5.6 mmol) was added to a stirred solution of 3-cyclobutyl-2,3,4,5-tetrahydro-1H-benzo[d]azepin-7-ol (E3) (868 mg, 4.0 mmol), 2,4-difluorobenzyl bromide (0.25 ml, 2.1 mmol) and potassium iodide (25 mg) in butanone (9 ml). The reaction mixture was stirred at reflux for 18 hours, cooled, filtered and concentrated in vacuo. The crude residue was dissolved with ethyl acetate and washed with water and brine. The organic layer was dried over magnesium sulfate, filtered and concentrated in vacuo. Purification of the resulting residue by column chromatography eluting with a mixture of 0.880 ammonia:ethanol:dichloromethane (0.25:2.25:97.5 then 1:9:10) afforded the title compound (E79); MS (ES+) m/e 344 [M+H]+.

후처리

  1. temperatureat reflux for 18 hours
  2. temperaturecooled
  3. filtrationfiltered
  4. concentrationconcentrated in vacuo
  5. dissolutionThe crude residue was dissolved with ethyl acetate
  6. washwashed with water and brine
  7. dry with materialThe organic layer was dried over magnesium sulfate
  8. filtrationfiltered
  9. concentrationconcentrated in vacuo
  10. customPurification of the resulting residue by column chromatography
  11. washeluting with a mixture of 0.880 ammonia:ethanol:dichloromethane (0.25:2.25:97.5

출처 및 근거

ORD 기록
ord-e5331eece0554b2aaba512fb9e24df07
출처 데이터셋
uspto-grants-2010_04
특허 번호
US07696193B2

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