HCID 58008894, compound → HCID 58158302, compound
Reaction equation
[OH:1][CH2:2][C:3]1[N:4]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=2[CH3:21])[C:5](=[O:14])[C:6]2[C:11]([CH:12]=1)=[CH:10][CH:9]=[CH:8][C:7]=2[CH3:13]>C(Cl)Cl.O=[Mn]=O>[CH3:13][C:7]1[CH:8]=[CH:9][CH:10]=[C:11]2[C:6]=1[C:5](=[O:14])[N:4]([C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=1[CH3:21])[C:3]([CH:2]=[O:1])=[CH:12]2Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
To a stirred solution of 3-(hydroxymethyl)-8-methyl-2-o-tolylisoquinolin-1(2H)-one 1609 (2.79 g, 10 mmol) in CH2Cl2 (200 mL), MnO2 (5 g) was added and the resulting mixture was stirred at reflux for 3 h. The mixture was allowed to cool to RT, and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel (10-50% EA/PE) to afford the product, 8-methyl-1-oxo-2-o-tolyl-1,2-dihydroisoquinoline-3-carbaldehyde 4101 (2.5 g, 90% yield) as a white solid.
Workup
- temperatureat reflux for 3 h
- concentrationconcentrated in vacuo
- customThe residue was purified by flash column chromatography on silica gel (10-50% EA/PE)
Sources & evidence
- ORD record
- ord-b3c639054f8a45b08c974402a3deede8
- Source dataset
- uspto-grants-2014_07
- Patent number
- US08785456B2
Reaction notes
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