HCID 12919381, compound → HCID 12837963, compound
Reaction equation
[CH3:1][N:2]([CH3:20])[S:3]([N:6]1[C:10]2[CH:11]=[C:12]([C:15]([NH:17]N)=[O:16])[CH:13]=[CH:14][C:9]=2[N:8]=[C:7]1[NH2:19])(=[O:5])=[O:4]>[Ni]>[CH3:1][N:2]([CH3:20])[S:3]([N:6]1[C:10]2[CH:11]=[C:12]([C:15]([NH2:17])=[O:16])[CH:13]=[CH:14][C:9]=2[N:8]=[C:7]1[NH2:19])(=[O:4])=[O:5]Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
The procedure of method B above was repeated with 2.5 g. of 1-dimethylaminosulfonyl-2-amino-6-benzimidazolecarboxylic acid hydrazide and 10 g. of Raney nickel to yield 1-dimethylaminosulfonyl-2-amino-6-benzimidazolecarboxamide, m.p. about 206°-208° C. A second crop was obtained from the mother liquors.
Sources & evidence
- ORD record
- ord-fa766724b8ad48f1b29df0d0fab59712
- Source dataset
- uspto-grants-1978_10
- Patent number
- US04118573
Reaction notes
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