Methylamine → HCID 19373123, compound
Reaction equation
[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[N:9]=[C:10]3[N:14]([C:15]=2[CH2:16][C:17]([O:19]CC)=O)[C:13]2[CH:22]=[CH:23][CH:24]=[CH:25][C:12]=2[NH:11]3)=[CH:4][CH:3]=1.[CH3:26][NH2:27]>CO>[CH3:26][NH:27][C:17](=[O:19])[CH2:16][C:15]1[N:14]2[C:10]([NH:11][C:12]3[CH:25]=[CH:24][CH:23]=[CH:22][C:13]=32)=[N:9][C:8]=1[C:5]1[CH:6]=[CH:7][C:2]([CH3:1])=[CH:3][CH:4]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
2 g of ethyl 2-(4-methylphenyl)-9H-imidazo[1,2-a]benzimidazole-3-acetate in 60 ml of methanol are treated with 60 ml of liquid methylamine, while stirring the mixture at room temperature for 16 h. The solvent is evaporated under reduced pressure. The residue is washed with water and recrystallized twice from N,N-dimethylformamide. 0.8 g of compound is finally isolated. Melting point: 303°-308° C. (decomposition).
Workup
- customThe solvent is evaporated under reduced pressure
- washThe residue is washed with water
- customrecrystallized twice from N,N-dimethylformamide
Sources & evidence
- ORD record
- ord-3199f77b998d44fcb987d7378f08097f
- Source dataset
- uspto-grants-1995_11
- Patent number
- US05466706
Reaction notes
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