HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(((2-Aminoethyl)thio)methyl)-5-methylimidazole → HCID 13137369, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(((2-Aminoethyl)thio)methyl)-5-methylimidazole | HCID 665568 | — |
| Reactant | HCID 13137349 | HCID 13137349 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 13137369 | HCID 13137369 | — |
Reaction Steps
A mixture of 2-(5-methyl-4-imidazolylmethylthio)ethylamine (1.37 g), 2-nitroamino-5-(6-dimethylaminomethyl-3-pyridylmethyl)-4-pyrimidone (2.28 g) in pyridine were heated under reflux for 22 hr. The pyridine (12 ml) was evaporated at reduced pressure yielding [2-(5-methyl-4-imidazolyl-methylthio)ethylamino]-5-(6-dimethylaminomethyl-3-pyridylmethyl)-4-pyrimidone as a brown oily residue washed with water by decantation. The residue was dissolved in dilute ethanolic hydrochloric acid and the excess of solvent evaporated at reduced pressure. The residue was recrystallised from methanol/dilute ethanolic hydrochloric acid and then twice from methanol/ethanol to yield the tetrahydrochloride (0.82 g) as a light buff solid m.p. 167°-170° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04388317 |
| Source dataset | uspto-grants-1983_06 |
| ORD ID | ord-a97e36f5930f4cd195796848c32c15fe |
| Source note | uspto-grants-1983_06 |