Hydrogen iodide → HCID 20200300, compound
Reaction equation
C[O:2][C:3]1[CH:29]=[N:28][C:6]2[N:7]([CH2:22][CH2:23][CH2:24][N:25]([CH3:27])[CH3:26])[C:8]3[CH:21]=[CH:20][CH:19]=[CH:18][C:9]=3[C:10]([C:12]3[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=3)=[N:11][C:5]=2[CH:4]=1.I>C(O)(=O)C>[OH:2][C:3]1[CH:29]=[N:28][C:6]2[N:7]([CH2:22][CH2:23][CH2:24][N:25]([CH3:26])[CH3:27])[C:8]3[CH:21]=[CH:20][CH:19]=[CH:18][C:9]=3[C:10]([C:12]3[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=3)=[N:11][C:5]=2[CH:4]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The title compound is prepared by reacting 3-methoxy-N,N-dimethyl-6-phenyl-11H-pyrido[2,3-b][1,4]benzodiazepine-11-propanamine with hydrogen iodide and glacial acetic acid.
Sources & evidence
- ORD record
- ord-a42b4808aa5f490f8ca037cc9d134350
- Source dataset
- uspto-grants-1984_05
- Patent number
- US04447361
Reaction notes
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