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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2195512Generated: November 2, 2026

Methanesulfonic Acid → 5-(Benzyloxy)-6-bromo-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole

https://huagongshe.com/reaction/2195512

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
Reactant3,4-dihydro-2H-pyranHCID 8080—
ReactantSodium BicarbonateHCID 516892—
Reactant5-(Benzyloxy)-6-bromo-1H-indazoleHCID 66767049—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product5-(Benzyloxy)-6-bromo-1-(tetrahydro-2H-pyran-2-yl)-1H-indazoleHCID 6676706642.3%

Reaction Steps

To a solution of 5-(benzyloxy)-6-bromo-1H-indazole (5 g, 16.5 mmol) in THF (30 mL) and DCM (30 mL) is added 3,4-dihydro-2H-pyran (3 mL, 32.8 mmol) and methanesulfonic acid (1 mL, 15.3 mmol). After the reaction mixture is stirred at RT for 2 hours, EtOAc (50 mL) and saturated aqueous NaHCO3 are added. The organic phase is separated, dried over MgSO4, and concentrated. The residue is purified by silica gel column chromatography eluting with PE:EtOAc (4:1) to give the desired product (2.7 g, 42.2% yield). MS (m/z): 387.0 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE043878E1
Source datasetuspto-grants-2012_12
ORD IDord-a57be06121fb40e490748c0b73eebc93
Source noteuspto-grants-2012_12