HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → 5-(4-Hydroxy-2-pyridylmethyl)-4-pyrimidone trihydrobromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | 2-[2-(5-Methyl-4-imidazolylmethylthio)ethylamino]-5-(4-methoxy-2-pyridylmethyl)-4-pyrimidone | HCID 12788678 | — |
| Product | 5-(4-Hydroxy-2-pyridylmethyl)-4-pyrimidone trihydrobromide | HCID 178419241 | — |
Reaction Steps
A mixture of 2-[2-(5-methyl-4-imidazolylmethylthio) ethylamino]-5-(4-methoxy-2-pyridylmethyl)-4-pyrimidone (0.97 g) and aqueous hydrobromic acid (48%, 20 ml) was boiled under reflux for 20 hours and evaporated to dryness. The residue was recrystallised from a mixture of ethanol and 2-propanol to give 2-]2-(5-methyl-4-imidazolylmethylthio) ethylamino]-5-(4-hydroxy-2-pyridylmethyl)-4-pyrimidone trihydrobromide, m.p. 167-169°. On recrystallisation from a mixture of ethanol and 2-propanol the melting point of the sample was lower owing to loss of hydrogen bromide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04255428 |
| Source dataset | uspto-grants-1981_03 |
| ORD ID | ord-b760dad965544ee88f1830d2420b59e9 |
| Source note | uspto-grants-1981_03 |