HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → N-(2-bromoethyl)-1,2,3,4-tetrahydro-2,3-dioxo-6-quinoxaline sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Bromoethylamine hydrobromide | HCID 2774217 | — |
| Reactant | 2,3-Dioxo-1,2,3,4-tetrahydroquinoxaline-6-sulfonyl chloride | HCID 4983738 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-(2-bromoethyl)-1,2,3,4-tetrahydro-2,3-dioxo-6-quinoxaline sulfonamide | HCID 53792021 | 33% |
Reaction Steps
20.49 g (0.1 mole) of 2-bromoethylamine hydrobromide and 4.00 g (0.1 mole) of sodium hydroxide are dissolved in 60 ml of water, and 7.82 g (0.03 mole) of 1,2,3,4-tetrahydro-2,3-dioxo-6-quinoxalinesulfonyl chloride are added to the solution, and the mixture is stirred at room temperature for 6 hours. Then it is allowed to stand for 16 hours. The separated crystals are filtered, washed successively with water and acetone, dried, dissolved in a slight amount of hot dimethyl sulfoxide and precipitated from the solution with water. Thus 3.44 g (33%) of N-(2-bromoethyl)-1,2,3,4-tetrahydro-2,3-dioxo-6-quinoxaline sulfonamide are obtained, m.p.: 261-266° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05912245 |
| Source dataset | uspto-grants-1999_06 |
| ORD ID | ord-19847b66b4cd41129897a1fdf91e43f8 |
| Source note | uspto-grants-1999_06 |