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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 487624Generated: October 30, 2026

Acetic Anhydride → HCID 53920834, compound

https://huagongshe.com/reaction/487624

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantEthyl AcetateHCID 8857—
ReactantHCID 53875970HCID 53875970—
SolventPyridineHCID 1049—
ProductHCID 53920834HCID 5392083462.7%

Reaction Steps

1-[3-(2-Phenylpyrazolo[1,5-a]pyridin-3-yl)acryloyl]-2-hydroxymethylpiperidine (trans isomer) (0.50 g) was added to a stirred solution of acetic anhydride (0.16 g) in pyridine (5 ml) at room temperature, and stirred at room temperature for 3 hours. Ethyl acetate was added to the reaction mixture and washed with 1N aqueous sodium hydroxide solution, water and saturated sodium chloride aqueous solution, then dried over magnesium sulfate and evaporated in vacuo. The residue was chromatographed on silica gel (50 g) with a mixture of chloroform and acetone (20:1) as an eluent. The fractions containing the objective compound were combined and evaporated in vacuo to give 1-[3-(2-phenylpyrazolo-[1,5-a]pyridin-3-yl)acryloyl]-2-acetoxymethylpiperidine (trans isomer) (0.35 g) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05296490
Source datasetuspto-grants-1994_03
ORD IDord-61fe11074a1b4e9dab48a8b3129e49d5
Source noteuspto-grants-1994_03