HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(((2-Aminoethyl)thio)methyl)-5-methylimidazole → 2-[2-(5-Methyl-4-imidazolylmethylthio)ethylamino]-5-(1-methyl-2-oxopyridin-4-ylmethyl)pyrimidin-4-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(((2-Aminoethyl)thio)methyl)-5-methylimidazole | HCID 665568 | — |
| Reactant | 2-Nitroamino-5-(1-methyl-2-oxopyridin-4-ylmethyl)pyrimidin-4-one | HCID 70354123 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-[2-(5-Methyl-4-imidazolylmethylthio)ethylamino]-5-(1-methyl-2-oxopyridin-4-ylmethyl)pyrimidin-4-one | HCID 70353946 | 55.5% |
Reaction Steps
2-(5-Methyl-4-imidazolylmethylthio)ethylamine (1.37 g) and 2-nitroamino-5-(1-methyl-2-oxopyridin-4-ylmethyl)pyrimidin-4-one (2.08 g) were refluxed in ethanol (10 ml) for 24 hours. The reaction mixture was cooled and evaporated under reduced pressure to afford a glassy residue which was washed with hot water yielding a white solid. This solid was filtered off, washed with water and recrystallised from methanol to yield 2-[2-(5-methyl-4-imidazolylmethylthio)ethylamino]-5-(1-methyl-2-oxopyridin-4-ylmethyl)pyrimidin-4-one (1.61 g); recrystallisation from aqueous methanol afforded the title compound, m.p. 202.5°-203.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04540699 |
| Source dataset | uspto-grants-1985_09 |
| ORD ID | ord-864a287d8d434674aac02d611e871574 |
| Source note | uspto-grants-1985_09 |