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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1629952Generated: October 30, 2026

Trifluoroacetic acid → HCID 178434437, compound

https://huagongshe.com/reaction/1629952

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant1-(4-methoxybenzyl)-3-methyl-5-(4-(4-methylpiperazin-1-yl)phenyl)-1H-pyrazolo[3,4-b]pyridineHCID 68388435—
SolventChloroformHCID 6212—
ProductHCID 178434437HCID 178434437—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a stirred solution of 1-(4-methoxybenzyl)-3-methyl-5-(4-(4-methylpiperazin-1-yl)phenyl)-1H-pyrazolo[3,4-b]pyridine (160) in CHCl3 (20 mL) was added trifluoroacetic acid (5 mL) and heated at 50° C. for 12 hours. After completion of the reaction the solvents were removed, diluted with cold water, pH was adjusted to 8 and the aqueous phase extracted with chloroform twice. The organic layer was washed with brine solution and dried over sodium sulphate and the solvent completely distilled off to get the crude product. The crude was passed through 100-200 mesh silica gel, eluting the pure compound in 10% MeOH/CHCl3 as pale yellow solid compound 161 (8 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08791112B2
Source datasetuspto-grants-2014_07
ORD IDord-ef5b9f228f244d42a6692d48cb203429
Source noteuspto-grants-2014_07