2-Methyl-5-vinylpyridine → HCID 57876007, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([N:9]2[CH2:22][CH2:21][C:12]3[NH:13][C:14]4[CH:15]=[CH:16][C:17]([CH3:20])=[CH:18][C:19]=4[C:11]=3[CH2:10]2)=[CH:5][CH:4]=1.[CH3:23][C:24]1[CH:29]=[CH:28][C:27]([CH:30]=[CH2:31])=[CH:26][N:25]=1.[OH-].[K+]>CN1C(=O)CCC1>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([N:9]2[CH2:22][CH2:21][C:12]3[N:13]([CH2:31][CH2:30][C:27]4[CH:26]=[N:25][C:24]([CH3:23])=[CH:29][CH:28]=4)[C:14]4[CH:15]=[CH:16][C:17]([CH3:20])=[CH:18][C:19]=4[C:11]=3[CH2:10]2)=[CH:5][CH:4]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
The title compound is prepared from a mixture of 2,3,4,5-tetrahydro-2(4-methoxyphenyl)-8-methyl-1H-pyrido[4,3-b]indole, 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-630b2b9434ea4a3eb26a4a123b63356a
- Source dataset
- uspto-grants-2015_04
- Patent number
- US08999978B2
Reaction notes
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