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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2177657Generated: October 29, 2026

Sodium hydride → (R)-tert-butyl 3-(6-chloropyrazin-2-yloxy)piperidine-1-carboxylate

https://huagongshe.com/reaction/2177657

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2,6-DichloropyrazineHCID 78504—
Reactant(R)-1-Boc-3-hydroxypiperidineHCID 1514398—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product(R)-tert-butyl 3-(6-chloropyrazin-2-yloxy)piperidine-1-carboxylateHCID 57502428—

Reaction Conditions

Temperature2.5 °C

Reaction Steps

Sodium hydride (225.6 g, 5.64 mol) is dispersed into THF (3 L) and the temperature is lowered to 0-5° C. A solution of (R)-3-hydroxy-1-boc piperidine (891.6 g, 4.43 mol) in THF (3 L) is added over 1 h while maintaining the temperature between 0-5° C. The reaction is stirred for 1 h. 2,6-Dichloropyrazine (600 g, 4.03 mol) as a solution in THE (3 L) is added dropwise over 1.5 h maintaining the same temperature. The reaction is stirred for 2 h at 25-30° C., and then poured onto ice. The mixture is diluted with water and extracted with ethyl acetate. The extracts are dried over anhydrous sodium sulfate, filtered, and concentrated. The residual oil is triturated with 5% dichloromethane in hexane to give the product as a white solid. The solid is collected by filtration and dried, to give 1538 g crude material. The crude product is retriturated with 5% dichloromethane in hexanes to give a white solid in quantitative yield. ES/MS m/z 314.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067920B2
Source datasetuspto-grants-2015_06
ORD IDord-f8c61b842ea94157805b83a93949f3e0
Source noteuspto-grants-2015_06