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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1050348Generated: October 30, 2026

Ethyl orthoformate → Pyrido[4,3-d]pyrimidin-4(3H)-one, 7-chloro-

https://huagongshe.com/reaction/1050348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl orthoformateHCID 31214—
Reactant1279815-28-9HCID 118598557—
SolventDiethyl EtherHCID 3283—
ProductPyrido[4,3-d]pyrimidin-4(3H)-one, 7-chloro-HCID 136980669—

Reaction Conditions

Temperature140 °C

Reaction Steps

4-Amino-6-chloro-pyridine-3-carboxamide (2, 4.5 g, 26.23 mmol) was added to a pressure tube and triethylorthoformate (30 mL) was added. The reaction vessel was sealed and heated to 140° C. for 11 h. After the cyclization was complete, the reaction mixture was concentrated under reduced pressure, and to the solid obtained was added diethyl ether. The solid was filtered, washed with diethyl ether and dried in vacuum to afford 7-chloro-3H-pyrido[4,3-d]pyrimidin-4-one (3) as brown solid. MS (ESI) m/z 181.90 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09382248B2
Source datasetuspto-grants-2016_07
ORD IDord-07f6b7946eda4e4398127e5ff5b53256
Source noteuspto-grants-2016_07