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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 261626Generated: October 27, 2026

4-(4-methyl-1H-imidazol-5-yl)butan-1-amine → 1-Methylthio-1-[4-(5-methylimidazol-4-yl)butylamino]-2-nitroethylene

https://huagongshe.com/reaction/261626

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(4-methyl-1H-imidazol-5-yl)butan-1-amineHCID 12769842—
Reactant1-Nitro2-methylthio-2-methylsulphinylethyleneHCID 54487094—
Product1-Methylthio-1-[4-(5-methylimidazol-4-yl)butylamino]-2-nitroethyleneHCID 7060794651%

Reaction Steps

Reaction of 4-(4-aminobutyl)-5-methylimidazole (see Example 7 (ii), 0.765 g, 0.005 mol) with 1-methylsulphinyl-1-methylthio-2-nitroethylene(0.91 g, 0.005 mol), gave 1-methylthio-1-[4-(5-methylimidazol-4-yl)butylamino]-2-nitroethylene (0.69 g, 51%) which was treated directly with methylamine to yield 1-methylamino-b 1-[4-(5-methylimidazol-4-yl)butylamino]-2-nitroethylene (0.40 g, 61.9%). This compound was reacted with picric acid to give 1-methylamino-1-[4-(5-methylimidazol-4-yl)butylamino]-2-nitroethylene picrate hemihydrate (0.33 g, 26.3% last stage), m.p. 185°-187°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04166184
Source datasetuspto-grants-1979_08
ORD IDord-411e41f02f0b4b12b5b3fab591e2cee7
Source noteuspto-grants-1979_08