Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pipemidic Acid | HCID 4831 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Nitrobenzyl bromide | HCID 66011 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22760701 | HCID 22760701 | 69.9% |
Reaction Steps
A mixture of 2.0 g of 2-(1-piperazinyl)-8-ethyl-5,8-dihydro-5-oxopyrido[2,3-d]pyrimidine-6-carboxylic acid, 1.34 g of triethylamine, 2.14 g of p-nitrobenzyl bromide, and 50 ml of dimethylformamide was heated at 90° C. for 14 hours with stirring and concentrated to dryness under reduced pressure. Addition of 50 ml of water to the residue resulted in the separation of a solid, which was collected and recrystallized from dimethylformamide to give the product (2.02 g), m.p. 259°-261° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04125615 |
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| Source dataset | uspto-grants-1978_11 |
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| ORD ID | ord-d9295f6f8c5640c49d674aa17e711b54 |
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| Source note | uspto-grants-1978_11 |
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