Water → HCID 178513086, compound
Reaction equation
Cl.[NH2:2][C:3]([NH2:5])=[NH:4].C[O-].[Na+].[NH2:9][C:10]1[C:11]([C:22]([O:24]C)=[O:23])=[N:12][C:13]([S:17][C:18]([F:21])([F:20])[F:19])=[C:14]([NH2:16])[N:15]=1.O>CO>[OH2:23].[C:3]([NH:5][C:22]([C:11]1[C:10]([NH2:9])=[N:15][C:14]([NH2:16])=[C:13]([S:17][C:18]([F:19])([F:20])[F:21])[N:12]=1)=[O:24])(=[NH:2])[NH2:4]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 25 °C
Procedure
Guanidine hydrochloride (3.34 g., 0.035 mole) is added to a solution of sodium methoxide (1.67 g., 0.032 mole) in methanol (20 ml.) with stirring at 25° C. After 15 minutes, methyl 3,5-diamino-6-trifluoromethylthio-2-pyrazinoate (1.85 g., 0.007 mole) is added, and the mixture is heated on a steam bath for 15 min. Crushed ice--H2O (20 ml.) is added to the reaction mixture to precipitate 390 mg. of N-amidino-3,5-diamino-6-trifluoromethylthio-2-pyrazinecarboxamide, m.p. 195° C.
Workup
- temperaturethe mixture is heated on a steam bath for 15 min
- customto precipitate 390 mg
Sources & evidence
- ORD record
- ord-63ab033c74f348989514258be4d73ca9
- Source dataset
- uspto-grants-1980_04
- Patent number
- US04196292
Reaction notes
Loading…