HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pipemidic Acid → HCID 22760702, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pipemidic Acid | HCID 4831 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Acetamide, N-(4-(bromomethyl)phenyl)- | HCID 149290 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22760702 | HCID 22760702 | 80.7% |
Reaction Steps
To a suspension of 35.3 g of 2-(1-piperazinyl)-8-ethyl-5,8-dihydro-5-oxopyrido[2,3-d]pyrimidine-6-carboxylic acid in 500 ml of dimethylformamide was added a solution of 39.0 g of potassium carbonate in 50 ml of water and then 39.5 g of p-acetamidobenzyl bromide. The mixture was heated at 80°-90° C. for 1.5 hours with stirring. After removal of a small amount of the insoluble material by filtration, the filtrate was concentrated to dryness under reduced pressure and the residue was dissolved in 100 ml of water. The solution was adjusted to pH 7.0 with acetic acid. The precipitate was collected by filtration and recrystallized from a mixture of dimethylformamide and ethanol to give the product (42.3 g), m.p. 216.5°-219° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04125615 |
| Source dataset | uspto-grants-1978_11 |
| ORD ID | ord-a212cb41d2154ec3a29fdf56e69e5e7b |
| Source note | uspto-grants-1978_11 |