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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 715029Generated: October 29, 2026

Trifluoroacetic acid → HCID 178434434, compound

https://huagongshe.com/reaction/715029

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 70811058HCID 70811058—
SolventChloroformHCID 6212—
ProductHCID 178434434HCID 178434434—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 1-(4-methoxybenzyl)-3-methyl-5-(3-((4-methylpiperazin-1-yl)methyl)phenyl)-1H-pyrazolo[3,4-b]pyridine (122) (30 mg, 0.136 mmol) dissolved in chloroform (25 mL) was added trifluoroacetic acid (6 mL) and the reaction mixture was heated at 50° C. for 12 h. After completion of the reaction the solvents were removed and diluted with cold water, pH was adjusted to 8 and the aqueous phase extracted with chloroform two times. The organic layer was washed with brine solution and dried over sodium sulphate and the solvents were removed. The crude was passed through 100-200 mesh silica gel eluting the compound at 7% MeOH/CHCl3 as pale yellow solid of 3-methyl-5-(3-((4-methylpiperazin-1-yl)methyl)phenyl)-1H-pyrazolo[3,4-b]pyridine 123 obtained in 10 mg quantity. MS m/z 322.1 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187473B2
Source datasetuspto-grants-2015_11
ORD IDord-c66dbe4a07e74797af887e815c650282
Source noteuspto-grants-2015_11