HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethylamine → 4-Diethylamino-1-n-propyl-[1,2,4]triazolo[4,3-a]quinoxaline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethylamine | HCID 8021 | — |
| Reactant | 4-Chloro-1-propyl[1,2,4]triazolo[4,3-a]quinoxaline | HCID 13385707 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Diethylamino-1-n-propyl-[1,2,4]triazolo[4,3-a]quinoxaline | HCID 13385719 | 78% |
Reaction Steps
4-Chloro-1-n-propyl-[1,2,4]-triazolo[4,3-a]quinoxaline (1.23 g., 0.005 mole), the product of Example 5, and 1.1 g. (0.015 mole) of diethylamine in N,N-dimethylformamide (15 ml.) were stirred at room temperature for 2 hours. The reaction mixture was then poured over ice. The precipitate was removed by filtration, washed with water and air dried. Recrystallization (twice) from ethanol/water afforded 1.1 g. (78% yield) of pure 4-diethylamino-1-n-propyl-[1,2,4]triazolo[4,3-a]quinoxaline, m.p. 92°-94° C. Mass spectrum: m/e, 283 (P).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04623725 |
| Source dataset | uspto-grants-1986_11 |
| ORD ID | ord-6e6295f455ec49c2b919e62d4e8b08dd |
| Source note | uspto-grants-1986_11 |