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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-(2-amino-5-fluorophenyl)aminomethanephosphonic acid diethyl ester | HCID 15281075 | — |
| Reactant | Oxalic acid monoethylester chloride | HCID 23618337 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (7-Fluoro-1,2,3,4-tetrahydro-2,3-dioxoquinoxalin-1-yl)-methanephosphonic acid diethyl ester | HCID 15281076 | 71.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05955461 |
|---|
| Source dataset | uspto-grants-1999_09 |
|---|
| ORD ID | ord-0e19008555514bb5888a7fb46b3d1e50 |
|---|
| Source note | uspto-grants-1999_09 |
|---|