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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine, 2-(trimethylsilyl)- | HCID 139573 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | Methyl 1-[(4-iodophenyl)sulfonyl]piperidine-4-carboxylate | HCID 43423387 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Catalyst | HCID 178418778 | HCID 178418778 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 1-{[4-(pyridin-2-yl)phenyl]sulfonyl}piperidine-4-carboxylate | HCID 58494546 | 50% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08609696B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-5d2c642126d34c0aaa4435ea72b96f65 |
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| Source note | uspto-grants-2013_12 |
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