Sulfuric Acid → HCID 89964173, compound
Reaction equation
[CH3:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[C:8](=[O:12])[N:7]([C:13]1[CH:14]=[N:15][CH:16]=[CH:17][C:18]=1[C:19]([F:22])([F:21])[F:20])[CH2:6][CH2:5]2.OS(O)(=O)=O.[N+:28]([O-])([O-:30])=[O:29].[K+]>>[CH3:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][C:11]=1[N+:28]([O-:30])=[O:29])[C:8](=[O:12])[N:7]([C:13]1[CH:14]=[N:15][CH:16]=[CH:17][C:18]=1[C:19]([F:20])([F:22])[F:21])[CH2:6][CH2:5]2Participants
4
Procedure
6-Methyl-2-(4-(trifluoromethyl)pyridin-3-yl)-3,4-dihydroisoquinolin-1(2H)-one (71A: 450 mg, 1.465 mmol) was reacted with concentrated H2SO4 (4.4 mL) and KNO3 (163 mg, 1.6126 mmol) for 2 hours to afford 350 mg of the product (68% yield).
Sources & evidence
- ORD record
- ord-c0aab4cf98c84d118713c96633ece227
- Source dataset
- uspto-grants-2015_02
- Patent number
- US08946260B2
Reaction notes
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