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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1913163Generated: October 27, 2026

Pyridine, 2-(trimethylsilyl)- → Methyl 1-{[4-(pyridin-2-yl)phenyl]sulfonyl}piperidine-4-carboxylate

https://huagongshe.com/reaction/1913163

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridine, 2-(trimethylsilyl)-HCID 139573—
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantMethyl 1-[(4-iodophenyl)sulfonyl]piperidine-4-carboxylateHCID 43423387—
CatalystHCID 178418397HCID 178418397—
CatalystHCID 178418778HCID 178418778—
SolventDimethylformamideHCID 6228—
ProductMethyl 1-{[4-(pyridin-2-yl)phenyl]sulfonyl}piperidine-4-carboxylateHCID 5849454650%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a stirred suspension of methyl 1-[(4-iodophenyl)sulfonyl]piperidine-4-carboxylate (1.97 g, 4.81 mmol) and 2-(trimethylsilyl)pyridine (2.0 mL), 14.5 mmol) in anhydrous N,N-dimethyl formamide (50 mL) is added silver (I) oxide (1.12 g, 4.82 mmol), tetrakis(triphenylphosphine)palladium (0.28 g, 5 mol %) and tetrabutyl ammonium fluoride (1M in THF, 0.48 mL). The reaction is heated at 90° C. for 18 h. The reaction mixture is filtered and washed with EtOAc. The filtrate is concentrated under reduced pressure. Purification by column chromatography (silica, eluent: heptane, 5-75% EtOAc) gives 0.87 g (50%) of methyl 1-{[4-(pyridin-2-yl)phenyl]sulfonyl}piperidine-4-carboxylate. m/z=361 [M++H].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609696B2
Source datasetuspto-grants-2013_12
ORD IDord-5d2c642126d34c0aaa4435ea72b96f65
Source noteuspto-grants-2013_12