HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1802159Generated: October 30, 2026
Triethylamine → 6-Methyl-2-phenyl-[1,2,4]triazolo[1,5-A]pyridin-7-amine
https://huagongshe.com/reaction/1802159
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Diphenylphosphoryl azide | HCID 123414 | — |
| Reactant | 6-Methyl-2-phenyl-[1,2,4]triazolo[1,5-a]pyridine-7-carboxylic acid | HCID 67776675 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | 6-Methyl-2-phenyl-[1,2,4]triazolo[1,5-A]pyridin-7-amine | HCID 67775113 | 28.2% |
Reaction Steps
To a suspension of 6-methyl-2-phenyl-[1,2,4]triazolo[1,5-a]pyridine-7-carboxylic acid (172 mg, 679 μmol) and triethylamine (206 mg, 284 μl, 2.04 mmol) in tert-butanol (10 ml) is added at 25° C. diphenyl phosphorazidate (220 μl, 1.02 mmol). The resulting mixture is heated to reflux and stirred for 18 hours. The crude material is loaded on silica and purified by flash chromatography on a 20 g silica column using heptane/ethyl acetate 10-100% as eluent affording 6-methyl-2-phenyl-[1,2,4]triazolo[1,5-a]pyridin-7-ylamine (43 mg, 28%) as an off-white solid. mp.: >250° C. MS: m/z=225.3 (M+H+). The hydrochloride can be prepared by stirring in tetrahydrofurane/6N hydrochloric acid in diethylether (1:6) for 2 hours and final evaporation to dryness. Light brown solid (quant.). MS: m/z=225.3 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08349824B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-83e76c29bdf2479b87b89adf2fd29838 |
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| Source note | uspto-grants-2013_01 |
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