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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1358231Generated: November 1, 2026

Diethyl Oxalate → (2-Methoxy-5-morpholin-4-yl-phenylamino)-thioxo-acetic acid

https://huagongshe.com/reaction/1358231

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl OxalateHCID 7268—
ReactantPhosphorus sulfide (P2S5)HCID 14817—
Reactant2-Methoxy-5-morpholinoanilineHCID 11367778—
ReactantHCID 21137088HCID 21137088—
SolventO-XyleneHCID 7237—
Product(2-Methoxy-5-morpholin-4-yl-phenylamino)-thioxo-acetic acidHCID 21919264—

Reaction Conditions

Temperature180 °C

Reaction Steps

In accordance with scheme 1, the compounds of formula I are prepared as follows: Diethyl oxalate (2) is heated to about 120° C. 2-Methoxy-5-morpholin-4-yl-phenylamine (1) is added very cautiously in small quantities and the mixture is heated for 90 minutes at about 180° C. After cooling to room temperature and filtration n-hexane is added. The resulting precipitate is collected by filtration. After washing with hexane and drying N-(2-methoxy-5-morpholin-4-yl-phenyl)-oxalamic acid ethyl ester (3) is obtained. Then, to the obtained compound of formula (3) in boiling xylene is added phosphorus pentasulfide in small portions over a period of about 30 minutes. The mixture is refluxed for about 5 hours, cooled to room temperature and filtered. The solution is extracted with 1N NaOH. The aqueous phase is washed with toluene, filtered, and treated at 0-5° C. with concentrated hydrochloric acid until pH 1 was reached. Filtration of the precipitate yielded (2-methoxy-5-morpholin-4-yl-phenylamino)-thioxo-acetic acid (4).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06596718B1
Source datasetuspto-grants-2003_07
ORD IDord-79284924ba0b468a8da2df95e109c531
Source noteuspto-grants-2003_07