1-Methylthio-1-methylamino-2-nitroethylene → HCID 131712379, compound
Reaction equation
[NH2:1][CH2:2][CH2:3][S:4][CH2:5][C:6]1[O:10][C:9]([CH2:11][NH:12][CH3:13])=[C:8]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[CH:7]=1.[CH3:20][NH:21][C:22](SC)=[CH:23][N+:24]([O-:26])=[O:25]>O>[OH2:10].[CH3:20][NH:21][C:22]([NH:1][CH2:2][CH2:3][S:4][CH2:5][C:6]1[O:10][C:9]([CH2:11][NH:12][CH3:13])=[C:8]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[CH:7]=1)=[CH:23][N+:24]([O-:26])=[O:25].[CH3:20][NH:21][C:22]([NH:1][CH2:2][CH2:3][S:4][CH2:5][C:6]1[O:10][C:9]([CH2:11][NH:12][CH3:13])=[C:8]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[CH:7]=1)=[CH:23][N+:24]([O-:26])=[O:25]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 5-[[2-(amino)ethyl]thio]methyl-N-methyl-3-phenyl-2-furanmethanamine (0.45 g) and N-methyl-1-(methylthio)-2-nitroethenamine (0.24 g) was stirred in water (5 ml) for 24 hours. The solvent was removed in vacuo and the residue purified by column chromatography (Silica/methanol) affording the title compound (0.3 g) as an amber glass.
Workup
- customThe solvent was removed in vacuo
- customthe residue purified by column chromatography (Silica/methanol)
Sources & evidence
- ORD record
- ord-7f94373ec7174466ae4671f59ef3195b
- Source dataset
- uspto-grants-1981_09
- Patent number
- US04288443
Reaction notes
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