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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 244677Generated: October 30, 2026

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

https://huagongshe.com/reaction/244677

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, available from Sinova Ltd) in dihydropyran (100 ml) was added TFA (0.068 ml) and the reaction was heated for 1.5 hours at reflux. After cooling, 180 ml DCM and 50 ml saturated sodium bicarbonate solution was added and stirred for 10 minutes. The DCM was separated from the aqueous 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 numberUS08658635B2
Source datasetuspto-grants-2014_02
ORD IDord-45c0eeb56bb9419b892f48e5f56eb30b
Source noteuspto-grants-2014_02