HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 131712642, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 70547666 | HCID 70547666 | — |
| Product | HCID 131712642 | HCID 131712642 | 59.9% |
Reaction Steps
2-trans-(2-phenyl-ethenyl)-3-methyl-6,7-methylen-4-oxo-4H-pyrido[1,2-a]pyrimidine-7-carboxylic acid (0.8 g) was reacted with methyl iodide (0.55 g) and anhydrous K2CO3 (0.65 g) in dmethylformamide (7 ml) under stirring at room temperature for 4 hours. After dilution with ice water the precipitate was filtered off: crystallization from acetone gave 0.5 g of 2-trans-(2-phenyl-ethenyl)-3-methyl-6,7-methylen-4-oxo-4H-pyrido[1,2-a]pyrimidine-7-carboxylic acid, methyl ester, m.p. 164°-165° C. By proceeding analogously the following compound were prepared:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04341780 |
| Source dataset | uspto-grants-1982_07 |
| ORD ID | ord-d6de7b3843ff4aef83b5edeea3c1ef36 |
| Source note | uspto-grants-1982_07 |