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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1517401Generated: November 3, 2026

Ethyl orthoformate → 7-Chloropyrido[3,2-d]pyrimidin-4(3H)-one

https://huagongshe.com/reaction/1517401

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl orthoformateHCID 31214—
Reactant3-Amino-5-chloropyridine-2-carboxamideHCID 21820058—
Product7-Chloropyrido[3,2-d]pyrimidin-4(3H)-oneHCID 135741637—

Reaction Steps

A suspension of 3-amino-5-chloro-pyridine-2-carboxamide (3.43 g, 20 mmole) in triethyl orthoformate (50 ml) was refluxed for 3 hours. After cooling to room temperature, the precipitate was collected by filtration and washed with hexane. The title compound was obtained as a white solid (3.4 g, yield 94%) which was characterized by its mass spectrum as follows: MS (m/z): 182.1 ([M+H]+, 100).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08232278B2
Source datasetuspto-grants-2012_07
ORD IDord-171b5364bd8a485b9ef57c9334802ff8
Source noteuspto-grants-2012_07