HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 2,3-dihydroxy-N-(2-methoxyethyl)quinoxaline-6-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 2-Methoxyethylamine | HCID 8018 | — |
| Reactant | 2,3-Dioxo-1,2,3,4-tetrahydroquinoxaline-6-sulfonyl chloride | HCID 4983738 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2,3-dihydroxy-N-(2-methoxyethyl)quinoxaline-6-sulfonamide | HCID 17598303 | 63% |
Reaction Steps
To a solution of 7.51 g (0.1 mole) of 2-methoxyethylamine in 20 ml of water 5.21 g (0.02 mole) of 1,2,3,4-tetrahydro-2,3-dioxo-6-quinoxalinesulfonyl chloride are added in small portions, under stirring, and the mixture is stirred at room temperature for 16 hours. It is allowed to stand further for 2 days, and then 15 ml of acetic acid and 10 ml of water are added to it. 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 3.80 g (63%) of 1,2,3,4-tetra-hydro-N-(2-methoxy-ethyl)-2,3-dioxo-6-quinoxaline sulfonamide are obtained, m.p.: 264-267° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05912245 |
| Source dataset | uspto-grants-1999_06 |
| ORD ID | ord-1146d7e83d974b508a18bc1f3798dcc3 |
| Source note | uspto-grants-1999_06 |