HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1953777Generated: November 2, 2026
Acetaldehyde → Dimethyl N-(7-Nitro-2,3-dimethoxyquinoxalin-5-ylmethyl)-alpha-aminoethylphosphonate
https://huagongshe.com/reaction/1953777
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetaldehyde | HCID 177 | — |
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sulfuric acid magnesium salt (1:1) | HCID 24083 | — |
| Reactant | 5-Aminomethyl-2,3-dimethoxy-7-nitro-quinoxaline | HCID 17915296 | — |
| Reactant | Dimethylphosphite | HCID 21884954 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Dimethyl N-(7-Nitro-2,3-dimethoxyquinoxalin-5-ylmethyl)-alpha-aminoethylphosphonate | HCID 23297975 | — |
Reaction Steps
500 mg (1.9 mmol) of 5-aminomethyl-7-nitro-2,3-dimethoxyquinoxaline, 834 mg (3.7 eq.) of magnesium sulfate, 335 mg (1.3 eq.) of potassium carbonate and 0.214 ml (2 eq.) of acetaldehyde are stirred at room temperature for 7 hours in 15 ml of dichloromethane. The reaction mixture is filtered off and the filtrate is evaporated. A solution of 0.32 ml (1.2 eq.) of triethylamine, 0.182 ml of dimethyl phosphite and 0.36 ml (1.5 eq.) of trimethylchlorosilane in 10 ml of dichloromethane is stirred at 0° for one hour, and the residue is added to 10 ml of dichloromethane and stirred for 14 hours. Water is added to the reaction mixture and the organic phase is separated off. The aqueous phase is extracted twice with dichloromethane and the combined organic phases are dried over magnesium sulfate. The title compound is obtained as a yellow resin after evaporation of the solvent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06117873 |
|---|
| Source dataset | uspto-grants-2000_09 |
|---|
| ORD ID | ord-bc2cd44919154f3abf6da06e70be51a8 |
|---|
| Source note | uspto-grants-2000_09 |
|---|