HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(4-methyl-1H-imidazol-5-yl)butan-1-amine → 1-Methylthio-1-[4-(5-methylimidazol-4-yl)butylamino]-2-nitroethylene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(4-methyl-1H-imidazol-5-yl)butan-1-amine | HCID 12769842 | — |
| Reactant | 1-Nitro2-methylthio-2-methylsulphinylethylene | HCID 54487094 | — |
| Product | 1-Methylthio-1-[4-(5-methylimidazol-4-yl)butylamino]-2-nitroethylene | HCID 70607946 | 51% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04166184 |
| Source dataset | uspto-grants-1979_08 |
| ORD ID | ord-411e41f02f0b4b12b5b3fab591e2cee7 |
| Source note | uspto-grants-1979_08 |