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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2192912Generated: October 31, 2026

Water → Tert-butyl {5-[2-(benzyloxy)ethoxy]pyrazin-2-yl}carbamate

https://huagongshe.com/reaction/2192912

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactanttert-ButanolHCID 6386—
ReactantTriethylamineHCID 8471—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant5-(2-Benzyloxyethoxy)pyrazine-2-carboxylic acidHCID 59571067—
ProductTert-butyl {5-[2-(benzyloxy)ethoxy]pyrazin-2-yl}carbamateHCID 59570995—

Reaction Steps

5-[2-(Benzyloxy)ethoxy]pyrazine-2-carboxylic acid (1.089 g) was suspended in tert-butyl alcohol (20 mL), and triethylamine (0.66 mL) and diphenylphosphoryl azide (0.9 mL) were added thereto. The reaction mixture was heated under reflux overnight and left to be cooled to room temperature. To the reaction mixture was added water, followed by extraction with ethyl acetate. The organic layer was sequentially washed with saturated aqueous sodium bicarbonate and saturated brine, and then dried over anhydrous magnesium sulfate. It was concentrated under reduced pressure, and the obtained crude product was purified by silica gel column chromatography (hexane:ethyl acetate=5:1-3:1) to obtain tert-butyl {5-[2-(benzyloxy)ethoxy]pyrazin-2-yl}carbamate (1.352 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329707B2
Source datasetuspto-grants-2012_12
ORD IDord-c220927ab80846d9856ac095201107d3
Source noteuspto-grants-2012_12