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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2101349Generated: October 31, 2026

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

https://huagongshe.com/reaction/2101349

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphosgeneHCID 94429—
ReactantWater TFA acetonitrileHCID 22145617—
Reactant4-Bromo-2-hydrazinyl-3-iodopyridineHCID 57799445—
SolventTetrahydrofuranHCID 8028—
Product7-bromo-8-iodo-[1,2,4]triazolo[4,3-a]pyridin-3(2H)-oneHCID 5779936897.1%

Reaction Conditions

Temperature20 °C

Reaction Steps

To a solution of triphosgene (91.7 g, 309 mmol) in THF (800 mL) was added 4-bromo-2-hydrazinyl-3-iodopyridine (32.3 g, 103 mmol) in several portions over 1 h at 20° C. The resulting reaction mixture was stirred for an additional 2 h at 20° C. The reaction was monitored by HPLC (acetonitrile-water-TFA) and completed in 2 h. The reaction mixture was cooled in ice bath and quenched by careful addition of H2O (800 mL). A large amount of solid was precipitated. This was filtered and successively washed with H2O (2×100 mL) and Et2O (100 mL). The filtrate was concentrated in vacuo to reduce volume by 50%. Newly formed solid was then filtered. This 2nd crop was also washed with H2O and Et2O. The two crops were combined and dried under high vacuum to obtain the title compound as a light beige solid (34 g, 100 mmol). MS: [M+H]+=337.9. 1H NMR (400 MHz, DMSO) δ 6.76 (d, J=7.03 Hz, 1H), 7.78 (d, J=7.47 Hz, 1H), 12.68 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07572808B2
Source datasetuspto-grants-2009_08
ORD IDord-8d4feb78d4f24b99924a3619e2b2349e
Source noteuspto-grants-2009_08