HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → [1,2,4]Triazolo[4,3-a]quinazoline, 7-chloro-1-methyl-5-phenyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | HCID 12246017 | HCID 12246017 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | [1,2,4]Triazolo[4,3-a]quinazoline, 7-chloro-1-methyl-5-phenyl- | HCID 1869146 | — |
Reaction Steps
In the next place, a solution of 0.5 g of the above-mentioned 5-chloro-2-(3-methyl-5-bromo-4H-1,2,4-triazol-4-yl)benzophenone in 20 ml of dimethylsulfoxide was heated, with stirring, at about 180° C for 10 hours, during which ammonia gas was continuously passed into the reaction mixture. After cooling, the reaction mixture was poured into ice-water and the resulting crystals were filtered, washed with water and dried. The crystals thus obtained was dissolved in chloroform and chromatographed on silica gel using chloroform as an eluent. The product thus separated was recrystallized from isopropyl ether to give 1-methyl-5-phenyl-7-chloro-s-triazolo[4,3-a]quinazoline, m.p. 325° - 327° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04002755 |
| Source dataset | uspto-grants-1977_01 |
| ORD ID | ord-f8f3a259f30945d793bd79cc3c95e98d |
| Source note | uspto-grants-1977_01 |