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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl Oxalate | HCID 7268 | — |
| Reactant | Phosphorus sulfide (P2S5) | HCID 14817 | — |
| Reactant | 2-Methoxy-5-morpholinoaniline | HCID 11367778 | — |
| Reactant | HCID 21137088 | HCID 21137088 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | (2-Methoxy-5-morpholin-4-yl-phenylamino)-thioxo-acetic acid | HCID 21919264 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06596718B1 |
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| Source dataset | uspto-grants-2003_07 |
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| ORD ID | ord-79284924ba0b468a8da2df95e109c531 |
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| Source note | uspto-grants-2003_07 |
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