2-Methyl-5-vinylpyridine → HCID 57876082, compound
Reaction equation
[OH:1][CH:2]1[C:7]2[NH:8][C:9]3[CH:10]=[CH:11][C:12]([CH3:15])=[CH:13][C:14]=3[C:6]=2[C:5](=[O:16])[N:4]([CH3:17])[CH2:3]1.[CH3:18][C:19]1[CH:24]=[CH:23][C:22]([CH:25]=[CH2:26])=[CH:21][N:20]=1.[OH-].[K+]>CN1C(=O)CCC1>[OH:1][CH:2]1[C:7]2[N:8]([CH2:26][CH2:25][C:22]3[CH:21]=[N:20][C:19]([CH3:18])=[CH:24][CH:23]=3)[C:9]3[CH:10]=[CH:11][C:12]([CH3:15])=[CH:13][C:14]=3[C:6]=2[C:5](=[O:16])[N:4]([CH3:17])[CH2:3]1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
The title compound is prepared from a mixture of 3,4-dihydro-4-hydroxy-2,8-dimethyl-2H-pyrido[4,3-b]indol-1(5H)-one, 2-methyl-5-vinylpyridine and KOH (5-7 equiv) in NMP at a temperature ranging between 25 deg C. to 100 deg C. The product obtained is isolated by preparative HPLC.
Workup
- customranging between 25 deg C
- customto 100 deg C
- customThe product obtained
- customis isolated by preparative HPLC
Sources & evidence
- ORD record
- ord-7358fcd0830448979ca144321b671d7e
- Source dataset
- uspto-grants-2015_04
- Patent number
- US08999978B2
Reaction notes
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