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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl 3-(3-chloropyrazin-2-yloxy)azetidine-1-carboxylate | HCID 58547798 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(Azetidin-3-yloxy)pyrazine | HCID 58547984 | 181% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09376450B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-c258c472d3f84adc93f248f5d618686b |
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| Source note | uspto-grants-2016_06 |
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