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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 590782Generated: October 29, 2026

Selenium Dioxide → 6-chloro-3-iodo-1-trityl-1H-pyrazolo[4,3-c]pyridine-4-carbaldehyde

https://huagongshe.com/reaction/590782

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSelenium DioxideHCID 24007—
Reactant6-chloro-3-iodo-4-methyl-1-trityl-1H-pyrazolo[4,3-c]pyridineHCID 118168962—
Solvent1,4-DioxaneHCID 31275—
Product6-chloro-3-iodo-1-trityl-1H-pyrazolo[4,3-c]pyridine-4-carbaldehydeHCID 11816895053.1%

Reaction Conditions

Temperature100 °C

Reaction Steps

6-Chloro-3-iodo-4-methyl-1-trityl-1H-pyrazolo[4,3-c]pyridine (20 g, 37.3 mmol) was dissolved in dioxane (400 mL) and selenium dioxide (12.43 g, 112 mmol) was added. The reaction mixture was stirred at 100° C. for 6 hrs. Selenium dioxide (4.14 g, 37.3 mmol) was added and the reaction mixture continued stirring at 100° C. overnight. The reaction was filtered over celite, rinsed with DCM, and concentrated in vacuo. The residue was dissolved in DCM (1.0 L) and filtered over celite. The material was concentrated in vacuo while loading on silica gel. Purification by flash chromatography (0-5% DCM/EtOAc) gave 6-chloro-3-iodo-1-trityl-1H-pyrazolo[4,3-c]pyridine-4-carbaldehyde (10.88 g, 19.79 mmol, 53.0%). 1H NMR (ppm, 500 MHz, DMSO-d6) δ 10.54 (s, 1H), 7.39-7.35 (m, 10H), 7.17-7.11 (m, 5H), 6.29 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09233979B2
Source datasetuspto-grants-2016_01
ORD IDord-299e10dbf97d4f3787a2f469f8d5c7c2
Source noteuspto-grants-2016_01