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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2101378Generated: October 25, 2026

Triphosgene → 8-bromo-7-(4-chlorophenyl)-5-methyl-[1,2,4]triazolo[4,3-a]pyridin-3(2H)-one

https://huagongshe.com/reaction/2101378

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphosgeneHCID 94429—
Reactant3-Bromo-4-(4-chlorophenyl)-2-hydrazinyl-6-methylpyridineHCID 57799459—
SolventTetrahydrofuranHCID 8028—
Product8-bromo-7-(4-chlorophenyl)-5-methyl-[1,2,4]triazolo[4,3-a]pyridin-3(2H)-oneHCID 5779940384%

Reaction Steps

To a solution of triphosgene (225 mg, 0.75 mmol) in anhydrous THF (2.5 mL) at 60° C. was added 3-bromo-4-(4-chlorophenyl)-2-hydrazinyl-6-methylpyridine (80 mg, 0.256 mmol) in small portions over 5 min. The resulting suspension was refluxed for 30 min. After cooling to room temperature, the reaction mixture was concentrated under reduced pressure to remove most of the THF. Water (5 mL) was added carefully to the remaining solution to destroy the excess triphosgene. The resulting aqueous suspension was stirred at room temperature for 30 min, then filtered. The collected solid was washed with water (5 mL×2), the hexanes, and dried in a 45° C. vacuum oven for 3 h to afford 70 mg (84%) of the title compound as a yellow solid. HPLC/MS: retention time=3.38 min, [M+H]+=338.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07572808B2
Source datasetuspto-grants-2009_08
ORD IDord-e2b5f7366e1f4238874ae2cdcc022f34
Source noteuspto-grants-2009_08