Hydrochloric Acid → HCID 18953926, compound
Reaction equation
[ClH:1].C(OC([NH:9][CH2:10][CH2:11][C:12]1[S:13][CH:14]=[C:15]([C:17]2[N:18]=[C:19]([N:22]=[C:23]([NH2:25])[NH2:24])[S:20][CH:21]=2)[N:16]=1)=O)(C)(C)C>C(O)C>[ClH:1].[ClH:1].[NH2:9][CH2:10][CH2:11][C:12]1[S:13][CH:14]=[C:15]([C:17]2[N:18]=[C:19]([N:22]=[C:23]([NH2:25])[NH2:24])[S:20][CH:21]=2)[N:16]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Hydrogen chloride gas was babbled to a solution of 4-[2-(2-t-butoxycarbonylaminoethyl)thiazol-4-yl]-2-(diaminomethyleneamino)thiazole (3.0 g) in ethanol (30 ml) for 10 minutes at room temperature. The mixture was stirred at room temperature for 20 minutes. The resulting precipitate was collected by filtration. Recrystallization from a mixture of methanol and diisopropyl ether afforded 4-[2-(2-aminoethyl)thiazol-yl]-2-(diaminomethyleneamino)thiazole dihydrochloride (2.3 g).
Workup
- filtrationThe resulting precipitate was collected by filtration
- customRecrystallization
- additionfrom a mixture of methanol and diisopropyl ether
Sources & evidence
- ORD record
- ord-08620f040e344ce0b1f91cced4ffcc3e
- Source dataset
- uspto-grants-1994_12
- Patent number
- US05371097
Reaction notes
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