Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1897936Generated: October 31, 2026

Trifluoroacetic acid → HCID 58097152, compound

https://huagongshe.com/reaction/1897936

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 86649623HCID 86649623—
SolventChloroformHCID 6212—
ProductHCID 58097152HCID 58097152—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 5.9 mg of tert-butyl 4-hydroxy-4-((6-(1,3-thiazol-2-ylamino)pyridin-2-yl)methyl)piperidine-1-carboxylate in 1 ml of chloroform was added 0.5 ml of trifluoroacetic acid at 0° C., followed by stirring the reaction mixture at 0° C. for 2 hours. The reaction mixture was concentrated in vacuo, basified with saturated aqueous sodium bicarbonate solution, and extracted with chloroform. The resulting chloroform layer was dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated in vacuo to give the title compound as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08519136B2
Source datasetuspto-grants-2013_08
ORD IDord-c2fd01fdf56d458abd121653e8948858
Source noteuspto-grants-2013_08