Hydrogen Bromide → HCID 178428167, compound
Reaction equation
C[O:2][C:3]1[N:12]([CH2:13][C:14]2[CH:19]=[CH:18][C:17]([C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][C:21]=3[C:26]3[NH:30][N:29]=[N:28][N:27]=3)=[CH:16][CH:15]=2)[C:6]2=[N:7][CH:8]=[CH:9][C:10]([CH3:11])=[C:5]2[N:4]=1.Br>O>[CH3:11][C:10]1[CH:9]=[CH:8][N:7]=[C:6]2[N:12]([CH2:13][C:14]3[CH:15]=[CH:16][C:17]([C:20]4[CH:25]=[CH:24][CH:23]=[CH:22][C:21]=4[C:26]4[NH:27][N:28]=[N:29][N:30]=4)=[CH:18][CH:19]=3)[C:3](=[O:2])[NH:4][C:5]=12Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 90 mg (0.23 mmol) of 2-methoxy-7-methyl-3[(2'-(1H-tetrazol-5-yl)-biphenyl-4-yl)methyl]-3H-imidazo[4.5-b]pyridine and 1 ml of 48% HBr was stirred at a room temperature for 1.5 hours. The product mixture was mixed with water to produce crystals, which was taken out and washed with water to obtain 70 mg of the intended compound.
Workup
- customto produce crystals, which
- washwashed with water
Sources & evidence
- ORD record
- ord-8d1ffcfe9c1e4361903e94ee57529047
- Source dataset
- uspto-grants-1996_04
- Patent number
- US05506238
Reaction notes
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