HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dipropylamine → 4-Di-n-propylamino-[1,2,4]triazolo[4,3-a]quinoxaline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dipropylamine | HCID 8902 | — |
| Reactant | 4-Chloro[1,2,4]triazolo[4,3-a]quinoxaline | HCID 1126118 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Di-n-propylamino-[1,2,4]triazolo[4,3-a]quinoxaline | HCID 13385710 | 41% |
Reaction Steps
4-Chloro-[1,2,4]triazolo[4,3-a]-quinoxaline (2.0 g., 0.01 mole), the product of Example 2, and 3.0 g. (0.03 mole) of di-n-propylamine in N,N-dimethylformamide (50 ml.) were stirred for 3 hours at room temperature. The solution was poured over ice to form a precipitate which was separated by filtration and air dried. Recrystallization from cyclohexane (250 ml.) afforded 1.1 g. (41% yield) of 4-di-n-propylamino-[1,2,4]triazolo[4,3-a]quinoxaline, m.p. 240°-242° C. Mass spectrum: m/e, 269 (P).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04547501 |
| Source dataset | uspto-grants-1985_10 |
| ORD ID | ord-b13ffa2b6e28429892396e89d11235d7 |
| Source note | uspto-grants-1985_10 |