Methylamine → HCID 12073478, compound
Reaction equation
[CH3:1][NH2:2].[F:3][C:4]1[CH:5]=[CH:6][C:7]2[C:8]3[C:17]([C:18]([O:20]CC)=O)=[N:16][N:15]([C:23]4[CH:24]=[N:25][CH:26]=[CH:27][CH:28]=4)[C:14](=[O:29])[C:9]=3[N:10]([CH3:13])[C:11]=2[CH:12]=1>ClCCl.CO>[F:3][C:4]1[CH:5]=[CH:6][C:7]2[C:8]3[C:17]([C:18]([NH:2][CH3:1])=[O:20])=[N:16][N:15]([C:23]4[CH:24]=[N:25][CH:26]=[CH:27][CH:28]=4)[C:14](=[O:29])[C:9]=3[N:10]([CH3:13])[C:11]=2[CH:12]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
A stream of gaseous methylamine is introduced into a solution of 0.28 g (0.76 mmol) of ethyl 7-fluoro-5-methyl-4-oxo-3-(pyridin-3-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxylate (obtained in stage 4.1.) in 30 ml of dichloromethane and 70 ml of methanol. Stirring is maintained for 4 h. The reaction medium is concentrated under reduced pressure. The residue is purified by chromatography on a column of silica gel (eluent: dichloromethane/methanol: 100/0 to 90/10). The solid obtained is recrystallized from a mixture of dichloromethane and ethyl acetate.
Workup
- temperatureis maintained for 4 h
- concentrationThe reaction medium is concentrated under reduced pressure
- customThe residue is purified by chromatography on a column of silica gel (eluent: dichloromethane/methanol: 100/0 to 90/10)
- customThe solid obtained
- customis recrystallized from a mixture of dichloromethane and ethyl acetate
Sources & evidence
- ORD record
- ord-2c2dda75e4014375b6cb5ccf3ce49ab1
- Source dataset
- uspto-grants-2009_08
- Patent number
- US07569567B2
Reaction notes
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