HCID 18953815, compound → HCID 18953827, compound
Reaction equation
[NH2:1][C:2](=[N:4][C:5]1[S:6][CH:7]=[C:8]([C:10]2[N:11]=[C:12]([C:15]([NH2:17])=[O:16])[S:13][CH:14]=2)[N:9]=1)[NH2:3].[ClH:18].O1CCOCC1>CO>[ClH:18].[NH2:1][C:2](=[N:4][C:5]1[S:6][CH:7]=[C:8]([C:10]2[N:11]=[C:12]([C:15]([NH2:17])=[O:16])[S:13][CH:14]=2)[N:9]=1)[NH2:3]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A suspension of 4-[2-(diaminomethyleneamino)thiazol-4-yl ]thiazole-2-carboxamide (1.0 g) in 4N-hydrogenchloride/dioxane (1.0 ml) and methanol (10 ml) was stirred for 1 hour at room temperature. The resulting precipitate was collected by filtration. Recrystallization from water afforded 4-[2-(diaminomethyleneamino)thiazol-4-yl)thiazole-2-carboxamide hydrochloride (850 mg).
Workup
- filtrationThe resulting precipitate was collected by filtration
- customRecrystallization from water
Sources & evidence
- ORD record
- ord-fe1c5d6e612d4f2a8ea845d384b20d09
- Source dataset
- uspto-grants-1994_12
- Patent number
- US05371097
Reaction notes
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