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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 715052Generated: October 29, 2026

Trifluoroacetic acid → HCID 178434465, compound

https://huagongshe.com/reaction/715052

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 68388571HCID 68388571—
SolventChloroformHCID 6212—
ProductHCID 178434465HCID 178434465—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a stirred solution of 2-(4-(3-((1-(4-methoxybenzyl)-3-methyl-1H-pyrazolo[3,4-b]pyridin-5-yl)amino)benzyl)piperazin-1-yl)ethanol (163) (50 mg, 0.103 mmol) in CHCl3 (10 mL) was added trifluoroacetic acid (6 mL) and the reaction mass heated at 60° C. overnight. After completion of the reaction the solvents were completely distilled off and diluted with water and the pH was adjusted to 9 and extracted with chloroform twice. The combined organic layer was washed with brine solution and dried over sodium sulphate and the solvents were removed and the crude material was passed through 100-200 mesh silica gel, eluting with 10% MeOH/CH2Cl2 obtained pure 2-(4-(3-((3-methyl-1H-pyrazolo[3,4-b]pyridin-5-yl)amino)benzyl)piperazin-1-yl)ethanol 164 as a pale yellow colored solid (6 mg). MS m/z 353.54 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187473B2
Source datasetuspto-grants-2015_11
ORD IDord-ac673e267f554098af6775403731dde1
Source noteuspto-grants-2015_11