HuagongsheHuagongshe Chemistry Print Report · For research reference only
Azane;hydrate → [1,2,4]Triazolo[4,3-a]quinazoline, 1-methyl-7-nitro-5-phenyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Azane;hydrate | HCID 12896473 | — |
| Reactant | HCID 21485917 | HCID 21485917 | — |
| Product | [1,2,4]Triazolo[4,3-a]quinazoline, 1-methyl-7-nitro-5-phenyl- | HCID 1864488 | — |
Reaction Steps
In the next place, a mixture of 0.8 g of 2-(2-acetylhydrazino)-4-phenyl-6-nitroquinazoline thus obtained and 16 g of polyphosphoric acid was heated at 150° to 160° C for 2 hours. The mixture was then poured into ice-water and made alkaline with concentrated ammonia water. The precipitated crystals were filtered, washed with ethanol and then recrystallized from chloroform to obtain 1-methyl-5-phenyl-7-nitro-s-triazolo[4,3-a]quinazoline as pale brown crystals, m.p. 350° - 352° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04002755 |
| Source dataset | uspto-grants-1977_01 |
| ORD ID | ord-497f79310f29445da908c0d1bf87134e |
| Source note | uspto-grants-1977_01 |