HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 2-Amino-1-carbethoxycarbonylmethyl-3-chloroquinoxalinium bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | 2,3-Dichloroquinoxaline | HCID 16659 | — |
| Reactant | Ethyl bromopyruvate | HCID 66144 | — |
| Reactant | 3-Chloroquinoxalin-2-amine | HCID 817274 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 2-Amino-1-carbethoxycarbonylmethyl-3-chloroquinoxalinium bromide | HCID 14067523 | — |
Reaction Steps
A solution of 9 g of 2-amino-3-chloro-quinoxaline [prepared by heating under pressure 2,3-dichloro-quinoxaline and ammonia in ethanol by method of Saikachi et al (Chem. Pharm. Bull. Tokyo (1961), Vol. 9, p. 941], 12 g of ethyl bromopyruvate and 180 ml of dimethoxy ethane was stirred overnight and was filtered to obtain 5.33 of 2-amino-1-carbethoxycarbonylmethyl-3-chloro-quinoxalinium bromide in the form of a pale yellow crystalline solid. The filtrate was held in a refrigerator for 2 days to obtain 2 more crops of 1.20 and 3.62 g of product for a total yield of 10.22 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04474784 |
| Source dataset | uspto-grants-1984_10 |
| ORD ID | ord-0572298f1fd24cb6b1e676d4ccd0d99b |
| Source note | uspto-grants-1984_10 |