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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1605158Generated: November 2, 2026

Pyridine → HCID 12070973, compound

https://huagongshe.com/reaction/1605158

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantButanoic acid, 4-chloro-4-oxo-, methyl esterHCID 73888—
ReactantMethyl 4-chloroanthranilateHCID 80001—
SolventBenzeneHCID 241—
ProductHCID 12070973HCID 12070973—

Reaction Steps

To the solution of 444 g of methyl 4-chloro-anthranilate in 1.3 lt of benzene and 199 ml of pyridine, that of 406 g of 3-carbomethoxy-propionyl chloride in 200 ml of benzene is added dropwise while stirring and cooling with ice. The mixture is stirred for 19 hours at room temperature, filtered and the filtrate evaporated. The combined residues are taken up in 3 lt of chloroform, the solution washed with water, 1 lt of N hydrochloric acid, 1 lt of 10% aqueous sodium bicarbonate and again with water, dried, filtered, evaporated and the residue recrystallized from acetonitrile, to yield the methyl N-(3-carbomethoxypropionyl)-4-chloroanthranilate melting at 80°-84°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03949081
Source datasetuspto-grants-1976_04
ORD IDord-f4a2a9e8cf77463885c0acf0fe3442f3
Source noteuspto-grants-1976_04