HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → Diethyl N-(2,3-dimethoxy-7-nitroquinoxalin-5-ylmethyl)-2-aminophenylphosphonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Diethyl (2-aminophenyl)phosphonate | HCID 12482984 | — |
| Reactant | 5-Bromomethyl-7-nitro-2,3-dimethoxyquinoxaline | HCID 23297983 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Diethyl N-(2,3-dimethoxy-7-nitroquinoxalin-5-ylmethyl)-2-aminophenylphosphonate | HCID 23297993 | — |
Reaction Steps
190 mg (0.579 mmol) of 5-bromomethyl-7-nitro-2,3-dimethoxyquinoxaline, 159 mg (1.2 eq.) of diethyl 2-aminophenylphosphonate and 0.2 ml (2 eq.) of diisopropylethylamine are stirred at reflux for 20 hours in 8 ml of acetonitrile. The reaction mixture is evaporated and the residue is extracted with water and ethyl acetate. The combined organic phases are dried using brine and magnesium sulfate and evaporated. The title compound is obtained as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06117873 |
| Source dataset | uspto-grants-2000_09 |
| ORD ID | ord-5c1987d5ec6240529002594ae1d4839e |
| Source note | uspto-grants-2000_09 |