Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 573311Generated: October 31, 2026

3-Chloro-N-methoxy-N-methylpyrazine-2-carboxamide → [4-(Benzyloxy)phenyl](3-chloropyrazin-2-yl)methanone

https://huagongshe.com/reaction/573311

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-N-methoxy-N-methylpyrazine-2-carboxamideHCID 53417529—
ReactantHCID 178419638HCID 178419638—
SolventTetrahydrofuranHCID 8028—
Product[4-(Benzyloxy)phenyl](3-chloropyrazin-2-yl)methanoneHCID 86688975—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 3-chloro-N-methoxy-N-methylpyrazine-2-carboxamide (2.05 g) in THF (50 mL) was added dropwise [4-(benzyloxy)phenyl]magnesium bromide in THF (12 mL) at 0° C. After stirring at 0° C. for 2 h, the mixture was quenched with water and extracted with AcOEt. The organic layer was washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (AcOEt/hexane) to give the title compound (2.47 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029536B2
Source datasetuspto-grants-2015_05
ORD IDord-c8087302b1f44c80af4ed5eeb2214e86
Source noteuspto-grants-2015_05