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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | 5-(2-Benzyloxyethoxy)pyrazine-2-carboxylic acid | HCID 59571067 | — |
| Product | Tert-butyl {5-[2-(benzyloxy)ethoxy]pyrazin-2-yl}carbamate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08329707B2 |
|---|
| Source dataset | uspto-grants-2012_12 |
|---|
| ORD ID | ord-c220927ab80846d9856ac095201107d3 |
|---|
| Source note | uspto-grants-2012_12 |
|---|