HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl bromopyruvate → 1-Carbethoxycarbonylmethyl-2-amino-6,7-dichloro-quinoxalinium bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl bromopyruvate | HCID 66144 | — |
| Reactant | 6,7-Dichloroquinoxalin-2-amine | HCID 14067518 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Carbethoxycarbonylmethyl-2-amino-6,7-dichloro-quinoxalinium bromide | HCID 20287978 | 26.2% |
Reaction Steps
A solution of 0.2 g of the product of Step A, 0.2 g of ethyl bromopyruvate and 15 ml of anhydrous tetrahydrofuran was stirred at room temperature for 24 hours and was filtered to obtain 0.1 g of 1-carbethoxycarbonylmethyl-2-amino-6,7-dichloro-quinoxalinium bromide as a pale yellow crystalline solid. The filtrate was allowed to stand for several days and was then filtered to obtain 0.065 g of the said compound as a yellowish brown solid for a total yield of 0.165 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04254123 |
| Source dataset | uspto-grants-1981_03 |
| ORD ID | ord-1c68248c28fc4b65a6ce56a23f06e1d9 |
| Source note | uspto-grants-1981_03 |