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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1781624Generated: October 30, 2026

Triethylamine → 4-chloro-N-(methoxycarbonylmethylthio)acetylanthranilic acid methyl ester

https://huagongshe.com/reaction/1781624

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethyl 4-chloroanthranilateHCID 80001—
ReactantMethyl [(2-chloro-2-oxoethyl)sulfanyl]acetateHCID 12361281—
SolventDichloromethaneHCID 6344—
Product4-chloro-N-(methoxycarbonylmethylthio)acetylanthranilic acid methyl esterHCID 22364774—

Reaction Steps

21.24 g (0.114 mol) of 4-chloroanthranilic acid methyl ester and 19.1 ml (0.137 mol) of triethylamine are placed in 180 ml of methylene chloride at 0°. A solution of 20.9 g (0.114 mol) of 2-(chloroformylmethylthio)-acetic acid methyl ester (T. Terasawa and T. Okada, J. Org. Chem., 42, 1163 (1977)) in 20 ml of methylene chloride is added dropwise thereto and the mixture is then stirred for 15 minutes at 0° and for 3 hours at room temperature. The reaction mixture is extracted with water and brine and the aqueous phases are washed with methylene chloride. The organic phases are combined, dried with sodium sulfate, filtered and concentrated. Chromatography of the crude product on silica gel with hexane/ethyl acetate (4:1) yields, in the form of yellowish crystals, 4-chloro-N-(methoxycarbonylmethylthio)acetylanthranilic acid methyl ester which is still impure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05633379
Source datasetuspto-grants-1997_05
ORD IDord-3c74e80b8099436f9d73ec980f6d944a
Source noteuspto-grants-1997_05