Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Chloroethanol | HCID 34 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 15574553 | HCID 15574553 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 15574554 | HCID 15574554 | 80.8% |
Reaction Steps
A mixture containing 5.0 g of ethyl 5,8-dihydro-2-(4-methyl-1-piperazinyl)-5-oxopyrido[2,3-d]pyrimidine-6-carboxylate, 70 ml of dimethylformamide, 0.90 g of 50% sodium hydride, and 3.8 g of ethylene chlorohydrin was heated at 100°C for one hour. Dimethylformamide was distilled off in vacuo, and the residue taken up in chloroform. The chloroform solution was washed with water, dried over anhydrous magnesium sulfate, and the solvent distilled off. The resulting solid was recrystallized from ethanol to yield 4.6 g of the product, m.p. 197° - 199°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03962443 |
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| Source dataset | uspto-grants-1976_06 |
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| ORD ID | ord-bf386cbe9b5a4c6797a2efd279856d8c |
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| Source note | uspto-grants-1976_06 |
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