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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 706964Generated: October 29, 2026

Cyclohexene → 6-((4-fluorotetrahydro-2H-pyran-4-yl)methoxy)pyridine-3-sulfonamide

https://huagongshe.com/reaction/706964

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexeneHCID 8079—
Reactant5-bromo-6-((4-fluorotetrahydro-2H-pyran-4-yl)methoxy)pyridine-3-sulfonamideHCID 67126452—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product6-((4-fluorotetrahydro-2H-pyran-4-yl)methoxy)pyridine-3-sulfonamideHCID 67126567—

Reaction Conditions

Temperature120 °C

Reaction Steps

To a suspension of 5-bromo-6-((4-fluorotetrahydro-2H-pyran-4-yl)methoxy)pyridine-3-sulfonamide (200 mg) and cyclohexene (0.549 mL) in ethyl acetate (10 mL) was added 10% palladium on carbon (57.6 mg). The suspension was stirred for 60 minutes at 120° C. The reaction mixture was filtered and concentrated. The product was purified by reverse-phase flash chromatography (C18, 15 g, 10%-100% acetonitrile/H2O/trifluoroacetic acid 0.1%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174982B2
Source datasetuspto-grants-2015_11
ORD IDord-9ff65150be9945e3ba9cd29e74be8d27
Source noteuspto-grants-2015_11