HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Acetylthiophene → 2-Methyl-7-(2-thienyl)-pyrido[2,3-d]pyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Acetylthiophene | HCID 6920 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4-Amino-2-methylpyrimidine-5-carbaldehyde | HCID 12904726 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-Methyl-7-(2-thienyl)-pyrido[2,3-d]pyrimidine | HCID 23353104 | 17% |
Reaction Steps
1 ml of 40% strength by weight aqueous potassium hydroxide solution was added to a suspension of 2.0 g (14.6 mmol) of 4-amino-5-formyl-2-methylpyrimidine and 1.93 g. (15.3 mmol) of 2-acetylthiophene in 25 ml of methanol. The reaction mixture was then stirred for 20 hours at 20°-25° C. after which the solvent was removed After the residue had been taken up in dichloromethane, the organic phase was washed with water, dried and evaporated down. Yield: 17%; mp.: 175°-180° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05597776 |
| Source dataset | uspto-grants-1997_01 |
| ORD ID | ord-7a9f5c9d3ce34332972a7aa089723b7c |
| Source note | uspto-grants-1997_01 |