Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 476571Generated: October 30, 2026

Acetic Anhydride → HCID 14423126, compound

https://huagongshe.com/reaction/476571

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 14423121HCID 14423121—
SolventPyridineHCID 1049—
ProductHCID 14423126HCID 1442312679.5%

Reaction Steps

To an ice-cooled solution of 6-chloro-2-oxo-1-{[4-(2-hydroxyethyl)-1-piperazinyl]carbonylmethyl]-1,2-dihydrothiazolo[5,4-b]pyridine (1.35 g) in dry pyridine (10 ml), acetic anhydride (0.73 g) was added dropwise and then the mixture was stirred at the temperature for 2 hours and at the room temperature for 4 hours. After removal of the solvent, the residual oil obtained was purified on an aluminum-oxide column chromatography using a mixture of chloroform and n-hexane (2:1). The fractions containing the objective compound were collected and evaporated to give crude crystals. The crude crystals were recrystallized from ethyl acetate to afford 6-chloro-2-oxo-1-{[4-(2-acetoxyethyl)-1-piperazinyl]carbonylmethyl}-1,2-dihydrothiazolo[5,4-b]pyridine (1,2 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04885297
Source datasetuspto-grants-1989_12
ORD IDord-aa805ceb73cf4fb68a4d6823a736590d
Source noteuspto-grants-1989_12