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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 715024Generated: October 30, 2026

Trifluoroacetic acid → HCID 178434436, compound

https://huagongshe.com/reaction/715024

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 70810921HCID 70810921—
SolventChloroformHCID 6212—
ProductHCID 178434436HCID 178434436—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 3-(1-(4-methoxybenzyl)-3-methyl-1H-pyrazolo[3,4-b]pyridin-5-yl)-N,N-dimethylbenzene-sulfonamide (110) (50 mg, 0.114 mmol) dissolved in chloroform (10 mL) was added trifluoroacetic acid (5 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 70% ethyl acetate in hexane as pale yellow solid N,N-dimethyl-3-(3-methyl-1H-pyrazolo[3,4-b]pyridin-5-yl)benzenesulfonamide 111 (30 mg). MS m/z 316.9 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187473B2
Source datasetuspto-grants-2015_11
ORD IDord-2a3b8c8d3acf4a8586db0e3a92c51d38
Source noteuspto-grants-2015_11