HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 436409Generated: October 29, 2026
Dimethylformamide → 1-Phenyl-3-isopropyl-2-oxo-1,2,3,4-tetrahydropyrido[2,3-d]pyrimidine
https://huagongshe.com/reaction/436409
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Isopropyl tosylate | HCID 598985 | — |
| Reactant | 1-Phenyl-3,4-dihydropyrido[2,3-d]pyrimidin-2(1H)-one | HCID 13259281 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-Phenyl-3-isopropyl-2-oxo-1,2,3,4-tetrahydropyrido[2,3-d]pyrimidine | HCID 13259287 | 256.8% |
Reaction Steps
To a solution of 4.5 g of 1-phenyl-2-oxo-1,2,3,4-tetrahydropyrido[2,3-d]pyrimidine and 50 ml of dry dimethylformamide was added 1.2 g of 50% sodium hydride and the mixture was stirred for 30 minutes at room temperature, and then heated to a temperature of 90° - 100° C. To this was gradually added 1.28 g of isopropyl p-toluenesulfonate and the whole was reacted for 1 hour. After the reaction was complete, the solvent was distilled off from the mixture under reduced pressure. The residue obtained was diluted with water to produce a crude precipitate, which was collected by filtration and then dissolved in ethyl ether. Separation and purification were accomplished by applying the solution on a column of alumina, and the eluate was concentrated to give 4.1 g of 1-phenyl-3-isopropyl-2-oxo-1,2,3,4-tetrahydropyrido[2,3-d]pyrimidine as colorless prisms, melting at 164° - 165° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04009166 |
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| Source dataset | uspto-grants-1977_02 |
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| ORD ID | ord-78439cc78e74466f86901672c9df7715 |
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| Source note | uspto-grants-1977_02 |
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