Hydrochloric Acid → HCID 18956299, compound
Reaction equation
[ClH:1].[C:2]([NH:5][CH2:6][C:7]1[S:8][CH:9]=[C:10]([C:12]2[N:13]=[C:14]([NH2:17])[S:15][CH:16]=2)[N:11]=1)(=[O:4])[CH3:3].C(OC(C)C)(C)C>CO>[ClH:1].[C:2]([NH:5][CH2:6][C:7]1[S:8][CH:9]=[C:10]([C:12]2[N:13]=[C:14]([NH2:17])[S:15][CH:16]=2)[N:11]=1)(=[O:4])[CH3:3]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
4N-Dioxanoic hydrogen chloride (10 ml) was added to a suspension of 4-(2-acetylaminomethylthiazol-4-yl)-2-aminothiazole (0.75 g) in methanol (30 ml). The mixture was stirred at room temperature for 40 minutes, and diisopropyl ether (50 ml) was added. The resulting precipitate was collected by filtration. Recrystallization from a mixture of methanol and dioxane afforded 4-(2-acetylaminomethylthiazol-4-yl)-2-aminothiazole hydrochloride (0.35 g).
Workup
- filtrationThe resulting precipitate was collected by filtration
- customRecrystallization
- additionfrom a mixture of methanol and dioxane
Sources & evidence
- ORD record
- ord-df8f0a8e7ba44abc837413f210993443
- Source dataset
- uspto-grants-1994_11
- Patent number
- US05364871
Reaction notes
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