HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Methylaziridine → N-(2,3-dimethoxy-7-nitro-quinoxalin-5-ylmethyl)-2-methylaziridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Methylaziridine | HCID 6377 | — |
| Reactant | Tetrabutylammonium Hydroxide | HCID 2723671 | — |
| Reactant | 5-Bromomethyl-7-nitro-2,3-dimethoxyquinoxaline | HCID 23297983 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(2,3-dimethoxy-7-nitro-quinoxalin-5-ylmethyl)-2-methylaziridine | HCID 18706571 | — |
Reaction Steps
200 mg (0.61 mmol) of 5-bromomethyl-2,3-dimethoxy-7-nitro-quinoxaline, 0.086 ml (2 equiv.) of propyleneimine and 0.295 ml (0.3 equiv.) of an aqueous 40% tetrabutylammonium hydroxide solution are stirred in 8 ml of dichloromethane for 20 hours at room temperature. The mixture is concentrated by evaporation and the residue is extracted with ethyl acetate and a 5% sodium carbonate solution. The combined organic phases are washed once with brine, dried over magnesium sulfate and concentrated by evaporation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06080743 |
| Source dataset | uspto-grants-2000_06 |
| ORD ID | ord-f364f529c1054243a41dc138abe5b97d |
| Source note | uspto-grants-2000_06 |