Hydrochloric Acid → HCID 18412414, compound
Reaction equation
[CH3:1][N:2]1[C:6]2[CH:7]=[CH:8][C:9]([S:11]([N:14]3[CH2:18][CH2:17][CH2:16][CH2:15]3)(=[O:13])=[O:12])=[CH:10][C:5]=2[N:4]=[C:3]1[CH2:19][O:20][C:21]1[CH:26]=[CH:25][CH:24]=[C:23]([C:27]#[N:28])[CH:22]=1.[ClH:29].C(=O)([O-])[O-].[NH4+:34].[NH4+]>C(O)C>[ClH:29].[CH3:1][N:2]1[C:6]2[CH:7]=[CH:8][C:9]([S:11]([N:14]3[CH2:15][CH2:16][CH2:17][CH2:18]3)(=[O:12])=[O:13])=[CH:10][C:5]=2[N:4]=[C:3]1[CH2:19][O:20][C:21]1[CH:26]=[CH:25][CH:24]=[C:23]([C:27](=[NH:34])[NH2:28])[CH:22]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Prepared analogously to Example 32 from 1-methyl-2-[(3-cyanophenyl)oxymethyl]-benzimidazol-5-yl-sulphonic acid-pyrrolidide, ethanolic hydrochloric acid, ethanol and ammonium carbonate.
Sources & evidence
- ORD record
- ord-30aaf5f53e21447e99910132ac152c97
- Source dataset
- uspto-grants-2002_10
- Patent number
- US06469039B1
Reaction notes
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