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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 618640Generated: October 31, 2026

Triethylamine → (7-Fluoro-1,2,3,4-tetrahydro-2,3-dioxoquinoxalin-1-yl)-methanephosphonic acid diethyl ester

https://huagongshe.com/reaction/618640

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantN-(2-amino-5-fluorophenyl)aminomethanephosphonic acid diethyl esterHCID 15281075—
ReactantOxalic acid monoethylester chlorideHCID 23618337—
SolventTetrahydrofuranHCID 8028—
Product(7-Fluoro-1,2,3,4-tetrahydro-2,3-dioxoquinoxalin-1-yl)-methanephosphonic acid diethyl esterHCID 1528107671.1%

Reaction Steps

660 mg of N(-2-amino-5-fluorophenyl)-aminomethanephosphonic acid diethyl ester is introduced in 70 ml of absolute tetrahydrofuran with 509 mg of triethylamine. A solution of 685 mg of oxalic acid ethyl ester chloride in 30 ml of tetrahydrofuran is slowly instilled into this solution. The batch is stirred for 4 hours at room temperature. After suctioning-off of the precipitated salts, the filtrate is concentrated by evaporation, boiled in a mixture of 23 ml of ethanol and 23 ml of 1 N hydrochloric acid for 2 hours at 110° C. bath temperature. It is evaporated to dryness and the residue is chromatographed on silica gel with methylene chloride:ethanol=10:1. 561 mg of (7-fluoro-1,2,3,4-tetrahydro-2,3-dioxoquinoxalin-1-yl)-methanephosphonic acid diethyl ester is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05955461
Source datasetuspto-grants-1999_09
ORD IDord-0e19008555514bb5888a7fb46b3d1e50
Source noteuspto-grants-1999_09