Hydrochloric Acid → 4-(5-Methyl-1-oxo-1,2-dihydro-isoquinolin-3-yl)-benzoic acid
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
- customthe reaction mixture irradiated
- customa microwave (300 W, 130° C., 20 min)
- customThe reaction mixtures
- customprecipitated out of solution
- filtrationThe solid was filtered
- washwashed with water
- customdried
- dissolutionThe solid was dissolved in DMF
- customto remove any residual palladium
- washeluting with DMF
- 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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