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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207798Generated: October 31, 2026

Benzyl 3-(3-chloropyrazin-2-yloxy)azetidine-1-carboxylate → 2-(Azetidin-3-yloxy)pyrazine

https://huagongshe.com/reaction/2207798

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl 3-(3-chloropyrazin-2-yloxy)azetidine-1-carboxylateHCID 58547798—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product2-(Azetidin-3-yloxy)pyrazineHCID 58547984181%

Reaction Steps

To a nitrogen-purged round bottomed flask was added benzyl 3-(3-chloropyrazin-2-yloxy)azetidine-1-carboxylate (see PREPARATION P20.1; 0.400 g, 0.688 mmol) and Pd/C (0.10 g, 0.094 mmol) and EtOH (10 mL). Hydrogen gas was bubbled through the solution for 1 minute, then a balloon of hydrogen gas was placed atop the round bottomed flask. After 30 minutes, the balloon was removed and the round bottomed flask sealed with a rubber septum. After 16 hours, the reaction was filtered through CELITE® and the cake was washed liberally with EtOAc. The filtrate was concentrated in vacuo to give crude 2-(azetidin-3-yloxy)pyrazine (0.188 g, 181% yield), as a off-white solid. The product was carried forward in the next step without further purification. MS (ESI) m/z 152.1 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376450B2
Source datasetuspto-grants-2016_06
ORD IDord-c258c472d3f84adc93f248f5d618686b
Source noteuspto-grants-2016_06