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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 606736Generated: October 30, 2026

Iodopyrazine → 4-(1-Phenyl-1-(pyrazin-2-yl)-methylene)-piperidine-1-carboxylic Acid tert-butyl Ester

https://huagongshe.com/reaction/606736

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodopyrazineHCID 642841—
Reactant4-(1-Bromo-1-phenyl-methylene)-piperidine-1-carboxylic Acid tert-butyl EsterHCID 59034585—
ReactantButyllithiumHCID 178418339—
CatalystZincchlorideHCID 3007855—
CatalystHCID 178418397HCID 178418397—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product4-(1-Phenyl-1-(pyrazin-2-yl)-methylene)-piperidine-1-carboxylic Acid tert-butyl EsterHCID 6704633468%

Reaction Steps

To a solution of 4-(1-bromo-1-phenyl-methylene)-piperidine-1-carboxylic acid tert-butyl ester (0.352 g, 1.0 mmol) in 4 mL of dry THF, at −78° C. under Ar, was added n-butyllithium solution (1.6M in hexanes, 0.75 mL, 1.2 mmol) dropwise. After 15 min, a solution of freshly fused ZnCl2 in 1.2 mL of dry THF was added dropwise and then the cooling bath was removed and the reaction mixture was allowed to warm to room temperature. To this mixture was then added 2-iodopyrazine (0.119 mL, 1.2 mmol) and (Ph3P)4Pd (0.058 g, 5 mol %) and the reaction vessel was sealed and then heated at 90° C. for 16 h. The cooled mixture was quenched with saturated aqueous NH4Cl and then it was partitioned with EtOAc-water. The organic phase was washed (brine), dried (Na2SO4) and evaporated to give a dark brown gum. Flash chromatography of this material [SiO2/1-2% MeOH—NH4OH (9:1) in CH2Cl2] afforded the title compound (0.237 g, 68%) as a light yellow solid:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915283B2
Source datasetuspto-grants-2011_03
ORD IDord-1069b061111246a595c2b721f67bb00e
Source noteuspto-grants-2011_03