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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodopyrazine | HCID 642841 | — |
| Reactant | 4-(1-Bromo-1-phenyl-methylene)-piperidine-1-carboxylic Acid tert-butyl Ester | HCID 59034585 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(1-Phenyl-1-(pyrazin-2-yl)-methylene)-piperidine-1-carboxylic Acid tert-butyl Ester | HCID 67046334 | 68% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07915283B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-1069b061111246a595c2b721f67bb00e |
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| Source note | uspto-grants-2011_03 |
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