HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 6-chloro-2-ethyl-1-(1-formamido-2,2,2-trichloroethyl)-1H-imidazo[4,5-b]quinoxaline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-(1,2,2,2-Tetrachloroethyl)formamide | HCID 19312 | — |
| Reactant | 6-chloro-2-ethyl-1H-imidazo[4,5-b]quinoxaline | HCID 178437541 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-chloro-2-ethyl-1-(1-formamido-2,2,2-trichloroethyl)-1H-imidazo[4,5-b]quinoxaline | HCID 21436010 | — |
Reaction Steps
To 240 ml of dry dimethylformamide warmed to 50° was added 3.5 parts of 6-chloro-2-ethyl-1H-imidazo[4,5-b]quinoxaline and 1.75 parts of triethylamine. The resulting solution was added, with stirring, to a 500 ml round-bottomed flask containing 3.3 parts of 1-formamido-1,2,2,2-tetrachloroethane and 45 parts of dry dimethylformamide at room temperature. After standing for 75 minutes, the clear solution was poured onto a mixture of 1500 parts of ice and water. The resulting solids were collected, washed with water and dried to give 4.6 parts of 6-chloro-2-ethyl-1-(1-formamido-2,2,2-trichloroethyl)-1H-imidazo[ 4,5-b]quinoxaline, decomposing at 109°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04022777 |
| Source dataset | uspto-grants-1977_05 |
| ORD ID | ord-b6a84695dae94eddb785bdd0ec374139 |
| Source note | uspto-grants-1977_05 |