HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Piperazinecarboxaldehyde → HCID 13089623, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Piperazinecarboxaldehyde | HCID 82191 | — |
| Reactant | 2-Chloro-5-oxo-6-carbethoxy-8-ethyl-5,8-dihydropyrido(2,3-d)pyrimidine | HCID 12266805 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 13089623 | HCID 13089623 | 83% |
Reaction Steps
A mixture of 8.4 g of 2-chloro-5-oxo-6-carbethoxy-8-ethyl-5,8-dihydro-pyrido(2,3-d)pyrimidine, 6.9 g of formylpiperazine and 160 cm3 of chloroform is heated under reflux for one hour. After cooling, the solution is washed with water and dried and the solvent is evaporated. The oily residue crystallises on being taken up in 100 cm3 of isopropyl ether. The solid is filtered off and recrystallised from 50 cm3 of ethanol and yields 8.9 g (82%) of 2-(4'-formylpiperazino)-5-oxo-6-carbethoxy-8-ethyl-5,8-dihydro-pyrido(2,3-d)pyrimidine which melts in two stages; melting point 195° C., solidification, followed by m.p. 204° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04034094 |
| Source dataset | uspto-grants-1977_07 |
| ORD ID | ord-f2f61e84d7d04c68bb859e5460c4a010 |
| Source note | uspto-grants-1977_07 |