HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(((2-Aminoethyl)thio)methyl)-5-methylimidazole → 2-[2-(5-Methyl-4-imidazolylmethylthio)ethyl-amino]-3-nitro-1,4,5,6-tetrahydropyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(((2-Aminoethyl)thio)methyl)-5-methylimidazole | HCID 665568 | — |
| Reactant | 2-Methylthio-3-nitro-1,4,5,6-tetrahydropyridine | HCID 12831745 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-[2-(5-Methyl-4-imidazolylmethylthio)ethyl-amino]-3-nitro-1,4,5,6-tetrahydropyridine | HCID 12831748 | 82% |
Reaction Steps
A solution of 2-(5-methyl-4-imidazolylmethylthio)ethylamine (0.51 g, 0.003 mol) and 2-methylthio-3-nitro-1,4,5,6-tetrahydropyridine (0.49 g, 0.003 mol) in ethanol (50 ml) was refluxed for 6 hours. The mixture was cooled, and the solvent was removed in vacuo. The residue was dissolved in hot propan-2-ol and the product crystallised on cooling. Recrystallisation of the product from propan-2-ol/methanol gave 2-[2-(5-methyl-4-imidazolylmethylthio)ethylamino]-3-nitro-1,4,5,6-tetrahydropyridine (0.66 g, 82%) m.p. 205.5°-206.5°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04324789 |
| Source dataset | uspto-grants-1982_04 |
| ORD ID | ord-b5526e0e5a034f469b31cd8f19105c74 |
| Source note | uspto-grants-1982_04 |