HCID 53759317, compound → HCID 12197399, compound
Reaction equation
[CH3:1][N:2]1[C:6]([CH:7]=[N:8][NH:9][C:10]([NH2:12])=[S:11])=[CH:5][N:4]=[C:3]1[N+:13]([O-:15])=[O:14]>O>[NH2:12][C:10]1[S:11][C:7]([C:6]2[N:2]([CH3:1])[C:3]([N+:13]([O-:15])=[O:14])=[N:4][CH:5]=2)=[N:8][N:9]=1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
2 Grams of 1-methyl-2-nitro-5-imidazolecarboxaldehyde thiosemicarbazone are added to a solution of 17.1 g. of FeNH4 (SO4)2. 12H2O in 35 ml. of water. The mixture is stirred at 80°-90° C. for 2 hours, and, after cooling, the solid product is collected on the filter and washed with water. The crude compound is crystallized from a mixture of methanol and dimethylformamide. Yield 0.95 g. (48%), m.p. 263°-265° C.
Workup
- temperatureafter cooling
- customthe solid product is collected on the
- filtrationfilter
- washwashed with water
- customThe crude compound is crystallized from a mixture of methanol and dimethylformamide
Sources & evidence
- ORD record
- ord-bb27abf1febd427dbdd47ddfc19f58ea
- Source dataset
- uspto-grants-1976_10
- Patent number
- US03987053
Reaction notes
Loading…