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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 520574Generated: October 29, 2026

Dichloromethane → 6-Bromo-4-nitro-2-(tetrahydro-2H-pyran-2-yl)-2H-indazole

https://huagongshe.com/reaction/520574

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTrifluoroacetic acidHCID 6422—
Reactant3,4-dihydro-2H-pyranHCID 8080—
ReactantSodium BicarbonateHCID 516892—
Reactant6-bromo-4-nitro-1H-indazoleHCID 24728059—
Product6-Bromo-4-nitro-2-(tetrahydro-2H-pyran-2-yl)-2H-indazoleHCID 58255818—

Reaction Steps

To 6-bromo-4-nitro-1H-indazole (10 g) in dihydropyran (100 ml) was added TFA (0.068 ml) and the reaction was heated for 1.5 h at reflux. After cooling, DCM (180 ml) and saturated sodium bicarbonate solution (50 ml) was added and stirred for 10 min. The DCM was separated from the aq which was re-washed with DCM (70 ml). The combined organic layers were passed through a hydrophobic frit and evaporated to dryness. The residual solid was triturated with ether then filtered. The solid material was dissolved in DCM and purified by chromatography on silica on the ISCO Companion, using an isocratic gradient of DCM. Purified fractions were combined and evaporated to dryness to afford the title compound, 7.78 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09326987B2
Source datasetuspto-grants-2016_05
ORD IDord-30df097a7307494eb8d09f158633fb60
Source noteuspto-grants-2016_05