5-Pyridin-4-yl-1,2,3,4-tetrahydro-isoquinoline → 5-(Pyridin-4-yl)-3,4-dihydroisoquinoline
Reaction equation
[N:1]1[CH:6]=[CH:5][C:4]([C:7]2[CH:16]=[CH:15][CH:14]=[C:13]3[C:8]=2[CH2:9][CH2:10][NH:11][CH2:12]3)=[CH:3][CH:2]=1>O=[Mn]=O>[N:1]1[CH:6]=[CH:5][C:4]([C:7]2[CH:16]=[CH:15][CH:14]=[C:13]3[C:8]=2[CH2:9][CH2:10][N:11]=[CH:12]3)=[CH:3][CH:2]=1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
Intermediate 17B was oxidized using MnO2. After 24 h, the reaction was filtered through Celite® and concentrated to afford 75 mg (80%) of Intermediate 17 as yellow oil. MS (ESI) m/z: 209.1 (M+H)+.
Workup
- filtrationthe reaction was filtered through Celite®
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-b1138b2b7d534b05a056bcc0b0e2f5f6
- Source dataset
- uspto-grants-2016_07
- Patent number
- US09394276B2
Reaction notes
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