Hydrochloric Acid → 4-(5-Methyl-1-oxo-1,2-dihydro-isoquinolin-3-yl)-benzoic acid

HRID 717092노트

반응식

HRID 717092 반응식
[CH3:1][C:2]1[CH:11]=[CH:10][CH:9]=[C:8]2[C:3]=1[CH:4]=[C:5]([C:13]1[CH:20]=[CH:19][C:16]([C:17]#N)=[CH:15][CH:14]=1)[NH:6][C:7]2=[O:12].[OH-:21].[Na+].Cl.[OH2:24]>>[CH3:1][C:2]1[CH:11]=[CH:10][CH:9]=[C:8]2[C:3]=1[CH:4]=[C:5]([C:13]1[CH:20]=[CH:19][C:16]([C:17]([OH:24])=[O:21])=[CH:15][CH:14]=1)[NH:6][C:7]2=[O:12]

참가 물질

5

실험 절차

To 4-(5-methyl-1-oxo-1,2-dihydro-isoquinolin-3-yl)-benzonitrile (100 mg, 0.38 mmol) was added 2M NaOH (1.5 mL) and the reaction mixture irradiated using a microwave (300 W, 130° C., 20 min). The reaction mixtures was diluted with water and adjusted to pH2 with 2M HCl whereupon a pale yellow solid precipitated out of solution. The solid was filtered, washed with water and dried. The solid was dissolved in DMF and passed through a Si-thiol cartridge to remove any residual palladium, eluting with DMF. The eluent was removed in vacuo to give 4-(5-methyl-1-oxo-1,2-dihydro-isoquinolin-3-yl)-benzoic acid as a pale yellow solid (120 mg, 63%).

후처리

  1. customthe reaction mixture irradiated
  2. customa microwave (300 W, 130° C., 20 min)
  3. customThe reaction mixtures
  4. customprecipitated out of solution
  5. filtrationThe solid was filtered
  6. washwashed with water
  7. customdried
  8. dissolutionThe solid was dissolved in DMF
  9. customto remove any residual palladium
  10. washeluting with DMF
  11. customThe eluent was removed in vacuo

출처 및 근거

ORD 기록
ord-3d09cb1ad1fb44f9bfcabac2baef7469
출처 데이터셋
uspto-grants-2015_11
특허 번호
US09193689B2

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