HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylamine → 4-Ethylamino-[1,2,4]triazolo[4,3-a]quinoxaline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylamine | HCID 6341 | — |
| Reactant | 4-Chloro[1,2,4]triazolo[4,3-a]quinoxaline | HCID 1126118 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Ethylamino-[1,2,4]triazolo[4,3-a]quinoxaline | HCID 13385709 | 32% |
Reaction Steps
A slurry of 2.0 g. (0.01 mole) of 4-chloro-[1,2,4]triazolo[4,3-a]quinoxaline (the product of Example 2) in N,N-dimethylformamide (30 ml.) was saturated with monoethylamine gas and stirred at room temperature for 2 hours. Monoethylamine gas was again bubbled through the mixture and stirring was continued for 2 hours. The precipitate was removed by filtration and washed with N,N-dimethylformamide. Recrystallization from methanol afforded 680 mg. (32% yield) 4-ethylamino-[1,2,4]triazolo[4,3-a]quinoxaline, m.p. 254°-256° C. Mass spectrum: m/e, 213 (P).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04547501 |
| Source dataset | uspto-grants-1985_10 |
| ORD ID | ord-44a7fdea810948d6b54a1d2b84d21fcf |
| Source note | uspto-grants-1985_10 |