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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376411Generated: October 25, 2026

Pyridine → 1-(2-Acetoxyethyl)-5-acetylaminopyrazole

https://huagongshe.com/reaction/1376411

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetic AnhydrideHCID 7918—
Reactant2-(5-amino-1H-pyrazol-1-yl)ethan-1-olHCID 320281—
ReactantSodium BicarbonateHCID 516892—
SolventEthyl AcetateHCID 8857—
SolventSodium chloride; waterHCID 57417360—
Product1-(2-Acetoxyethyl)-5-acetylaminopyrazoleHCID 22916765—

Reaction Steps

1-(2-Hydroxyethyl)-5-aminopyrazole (5 g) was added to acetic anhydride (14.7 ml) under stirring and ice-cooling, and pyridine (6.3 ml) was added thereto. The mixture was stirred for 2 hours at 25° C. The reaction mixture was added to a mixture of ethyl acetate (50 ml) and brine (50 ml). Then, the mixture was adjusted to pH 7.0 with an aqueous solution of sodium bicarbonate. The aqueous layer was extracted with a mixture of ethyl acetate and tetrahydrofuran. The extract was dried over magnesium sulfate. The magnesium sulfate was filtered off, and the filtrate was evaporated under reduced pressure to give 1-(2-acetoxyethyl)-5-acetylaminopyrazole (5.98 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05663163
Source datasetuspto-grants-1997_09
ORD IDord-03b639c79c4f4bd4a2742ffe81493c62
Source noteuspto-grants-1997_09