HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 434638Generated: October 30, 2026
Sodium Carbonate → HCID 20491752, compound
https://huagongshe.com/reaction/434638
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Isoxazole, 4-(chloromethyl)-3,5-dimethyl- | HCID 88246 | — |
| Reactant | 5-Chloropyrimidin-2-ol hydrochloride | HCID 12648523 | — |
| Catalyst | Benzyltrimethylammonium chloride | HCID 5963 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 20491752 | HCID 20491752 | 32.6% |
Reaction Steps
A mixture of 5-chloropyrimidin-2-one hydrochloride (0.668 g), 4-chloromethyl-3,5-dimethylisoxazole (0.874 g), anhydrous sodium carbonate (1.272 g) and benzyltrimethylammonium chloride (15 mg) in dimethylformamide (20 ml) was stirred and heated at 90° C. After 2.25 h the reaction mixture was diluted with water (200 ml) and extracted with ethyl acetate (100 ml, 2×50 ml). The combined extracts were washed with water (50 ml) and brine (50 ml), dried (MgSO4) and evaporated to an orange crystalline solid (0.811 g). The solid was subjected to preparative layer chromatography (p.l.c.) on silica developing with chloroform-ethyl acetate (1:1) (two runs). The major band was eluted with chloroform-ethanol (1:1) (three times) to give a cream crystalline solid (0.313 g) which was recrystallised from ethanol to give the title pyrimidone (0.189 g) m.p. 218°-219° C. (Kofler), λmax (EtOH) 225 nm (ε 9,300), 310 nm (ε 2,200) inflection at 245 nm (ε 4,300) νmax (CHBr3) 1677 cm-1 (C=O), (Nujol) 1668 cm-1 (C=O).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04399140 |
|---|
| Source dataset | uspto-grants-1983_08 |
|---|
| ORD ID | ord-173a9656d0ca47809ff36414d4e0908e |
|---|
| Source note | uspto-grants-1983_08 |
|---|