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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1042117Generated: November 3, 2026

2-[(Methylsulfonyl)methyl]-5-[4-nitro-3-(tetrahydro-2H-pyran-4-yloxy)phenoxy]pyridine → 4-({6-[(Methylsulfonyl)methyl]pyridin-3-yl}oxy)-2-(tetrahydro-2H-pyran-4-yloxy)aniline

https://huagongshe.com/reaction/1042117

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-[(Methylsulfonyl)methyl]-5-[4-nitro-3-(tetrahydro-2H-pyran-4-yloxy)phenoxy]pyridineHCID 66726224—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
Product4-({6-[(Methylsulfonyl)methyl]pyridin-3-yl}oxy)-2-(tetrahydro-2H-pyran-4-yloxy)anilineHCID 66726162100%

Reaction Steps

To a solution of 2-[(methylsulfonyl)methyl]-5-[4-nitro-3-(tetrahydro-2H-pyran-4-yloxy)phenoxy]pyridine (22 g) in ethanol (250 mL) was added 10% palladium carbon (2 g), and the mixture was stirred under a hydrogen atmosphere at room temperature for 15 hr. Palladium carbon was removed, and the residue was concentrated under reduced pressure to give the title compound (20 g, yield 100%) as a colorless amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08557805B2
Source datasetuspto-grants-2013_10
ORD IDord-84b8d44a75bb4f03baf5020423443b20
Source noteuspto-grants-2013_10