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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2407253Generated: October 30, 2026

Stannanecarbonitrile, tributyl- → 3-{(R*)-1-[(S)-1-(2,3-Dihydrobenzo[1,4]dioxin-2-yl)methyl]-piperidin-3-yl}-benzonitrile

https://huagongshe.com/reaction/2407253

Reaction equation

Participants

RoleNameHCIDCharge
ReactantStannanecarbonitrile, tributyl-HCID 200512—
ReactantTrifluoromethanesulfonic acid 3-{(R*)-1-[(S)-1-(2,3-dihydrobenzo[1,4]dioxin-2-yl)methyl]-piperidin-3-yl}phenyl esterHCID 86644712—
CatalystHCID 178418397HCID 178418397—
Solvent1,2-DichloroethaneHCID 11—
Product3-{(R*)-1-[(S)-1-(2,3-Dihydrobenzo[1,4]dioxin-2-yl)methyl]-piperidin-3-yl}-benzonitrileHCID 251751677.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of trifluoromethanesulfonic acid 3-{(R*)-1-[(S)-1-(2,3-dihydrobenzo[1,4]dioxin-2-yl)methyl]-piperidin-3-yl}phenyl ester (51 mg, 0.11 mmol), tributyltin cyanide (142 mg, 0.45 mmol) and tetrakis(triphenylphosphine)palladium (189 mg, 0.164 mmol) in 1,2-dichloroethane (15 ml) was heated in a microwave reactor at 80° C. for 80 h. The solid precipitate was filtered off and the mixture was evaporated to dryness. The residue was redissolved in DCM, filtered and washed two times with 1 M HCl. The combined organic phases were washed with brine, dried (Na2SO4) and evaporated to dryness. The crude product was purified by flash chromatography first using gradient of DCM and MeOH and then using gradient of heptane and EtOAc as eluent to give 2.8 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809536B2
Source datasetuspto-grants-2014_08
ORD IDord-3f7c493fe1484b4bad77ca6915e37687
Source noteuspto-grants-2014_08