Allylamine → HCID 178457594, compound
Reaction equation
[ClH:1].[C:2]([NH:5][C:6](=[NH:9])OC)(=[NH:4])[NH2:3].[CH2:10]([NH2:13])[CH:11]=[CH2:12]>C(O)C>[ClH:1].[CH2:10]([NH:13][C:6]([NH:5][C:2]([NH2:4])=[NH:3])=[NH:9])[CH:11]=[CH2:12]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Into 3 ml of ethanol were dissolved 5 g of guanyl-O-methylisourea hydrochloride and 3 ml of allylamine. The resulting solution was reacted at room temperature for 24 hours in a nitrogen stream. The reaction mixture was then filtered and the precipitates were washed with ethanol to give 3.14 g of allylbiguanide hydrochloride as needle like crystals (m.p.: 178°-179° C.).
Workup
- customThe resulting solution was reacted at room temperature for 24 hours in a nitrogen stream
- filtrationThe reaction mixture was then filtered
- washthe precipitates were washed with ethanol
Sources & evidence
- ORD record
- ord-f4a5fceb7d3d46e0900136496b5df6fd
- Source dataset
- uspto-grants-1997_09
- Patent number
- US05665843
Reaction notes
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