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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantDiphenylphosphoryl azideHCID 123414—
Reactant6-Methyl-2-phenyl-[1,2,4]triazolo[1,5-a]pyridine-7-carboxylic acidHCID 67776675—
Solventtert-ButanolHCID 6386—
Product6-Methyl-2-phenyl-[1,2,4]triazolo[1,5-A]pyridin-7-amineHCID 6777511328.2%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349824B2
Source datasetuspto-grants-2013_01
ORD IDord-83e76c29bdf2479b87b89adf2fd29838
Source noteuspto-grants-2013_01