HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → Ethyl 4-aminopyrazolo[1,5-a]quinoxaline-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | HCID 92039457 | HCID 92039457 | — |
| Product | Ethyl 4-aminopyrazolo[1,5-a]quinoxaline-3-carboxylate | HCID 71390467 | — |
Reaction Steps
2,76 g. of the chloro compound of Example 1 c is stirred for 10 hours with 25 ml. of saturated alcoholic ammonia solution at room temperature. The product, 4-aminopyrazolo[1,5-a]quinoxaline-3-carboxylic acid, ethyl ester, is obtained as a white precipitate which is filtered under suction, treated with water and recrystallized from ethanoldimethylformamide; yield 1.76 g., m.p. 235°-237°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04022782 |
| Source dataset | uspto-grants-1977_05 |
| ORD ID | ord-ad05fc15af094ca5b739e3090421d59c |
| Source note | uspto-grants-1977_05 |