Methylamine → HCID 178484396, compound
Reaction equation
[Br:1][C:2]1[NH:6][CH:5]=[N:4][C:3]=1[CH2:7][CH2:8][CH2:9][CH2:10][NH2:11].[N+](C=C(SC)SC)([O-])=O.[N+:21]([CH:24]=[C:25](SC)[NH:26][CH2:27]CCCC1N=CNC=1Br)([O-:23])=[O:22].CN>>[N+:21]([CH:24]=[C:25]([NH:26][CH3:27])[NH:11][CH2:10][CH2:9][CH2:8][CH2:7][C:3]1[N:4]=[CH:5][NH:6][C:2]=1[Br:1])([O-:23])=[O:22]Participants
5
Procedure
When 5-bromo-4-(4-aminobutyl)imidazole is reacted with 1-nitro-2,2-bis-methylthioethylene according to the procedure of Example 8(i) and the resultant 1-nitro-2-methylthio-2-[4-(5-bromo-4-imidazolyl)butylamino]ethylene, m.p. 157°-158° treated with methylamine by the procedure of Example 8(ii), the title compound, m.p. 145°-148° is produced.
Sources & evidence
- ORD record
- ord-08bd246eb5e248a2991a5c4b206dc606
- Source dataset
- uspto-grants-1979_05
- Patent number
- US04153704
Reaction notes
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