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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1605255Generated: October 30, 2026

1-Piperazinecarboxaldehyde → HCID 13089623, compound

https://huagongshe.com/reaction/1605255

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PiperazinecarboxaldehydeHCID 82191—
Reactant2-Chloro-5-oxo-6-carbethoxy-8-ethyl-5,8-dihydropyrido(2,3-d)pyrimidineHCID 12266805—
SolventChloroformHCID 6212—
ProductHCID 13089623HCID 1308962383%

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 1 hour. After cooling, the solution is washed with water and dried and the solvent is evaporated. The oily residue crystallises on being taken up to 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03950338
Source datasetuspto-grants-1976_04
ORD IDord-a3aca5c0aa4140d2954c081215f3df80
Source noteuspto-grants-1976_04