HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl chloride → 7-Bromo-2-phenyl-[1,2,4]triazolo[1,5-A]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | 1,2-Diamino-4-bromo-pyridinium 2,4,6-trimethyl-benzenesulfonate | HCID 86666016 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 7-Bromo-2-phenyl-[1,2,4]triazolo[1,5-A]pyridine | HCID 67775500 | 61.6% |
Reaction Steps
1,2-Diamino-4-bromopyridinium 2,4,6-trimethylbenzenesulfonate (15.6 g, 40.2 mmole) in pyridine (106 ml) is heated overnight at 100° C. with benzoyl chloride (9.4 ml, 80 mmole) giving a redbrown solution and after 2 hrs a brown suspension. The reaction mixture is concentrated in vacuo and the residue is triturated for 2.5 hr in sat. aqueous ammonium chloride solution (300 ml), while neutralizing to pH 6-7 with sat. aqueous sodium bicarbonate solution. The solid is collected by filtration, washed with water (40 ml) and dried affording 7-bromo-2-phenyl-[1,2,4]triazolo[1,5-a]pyridine (6.78 g, 61.6%) as an off-white solid. mp.: 189-191° C. MS: m/z=276.1, 274.2 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08349824B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-e460e77290b8486993baab1c4b133493 |
| Source note | uspto-grants-2013_01 |