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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 606737Generated: October 31, 2026

2-(Tributylstannyl)-1,3-thiazole → 4-(1-Phenyl-1-(thiazol-2-yl)-methylene)-piperidine-1-carboxylic Acid tert-butyl Ester

https://huagongshe.com/reaction/606737

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Tributylstannyl)-1,3-thiazoleHCID 2763259—
Reactant4-(1-Bromo-1-phenyl-methylene)-piperidine-1-carboxylic Acid tert-butyl EsterHCID 59034585—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
Product4-(1-Phenyl-1-(thiazol-2-yl)-methylene)-piperidine-1-carboxylic Acid tert-butyl EsterHCID 6704671394.3%

Reaction Conditions

Temperature90 °C

Reaction Steps

A solution of 4-(1-bromo-1-phenyl-methylene)-piperidine-1-carboxylic acid tert-butyl ester (0.205 g, 0.58 mmol) and 2-(tri-n-butylstannyl)thiazole (0.239 g, 0.64 mmol) in 6 mL of dry DMF was degassed with a stream of Ar bubbles for 10 min. To this solution was added (Ph3P)4Pd (0.067 g, 10 mol %) and CuI (0.011 g, 10 mol %), and then the reaction vessel was sealed and heated at 90° C. for 18 h. The cooled mixture was concentrated and then it was partitioned with EtOAc-water. The organic phase was washed (brine), dried (MgSO4) and evaporated. Flash chromatography of the residue (SiO2/hexane-EtOAc, 3:2) afforded the title compound (0.195 g, 94%) as a yellow solid:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915283B2
Source datasetuspto-grants-2011_03
ORD IDord-ba76ded471c542539f4803316ee804ae
Source noteuspto-grants-2011_03