HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 715052Generated: October 29, 2026
Trifluoroacetic acid → HCID 178434465, compound
https://huagongshe.com/reaction/715052
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 68388571 | HCID 68388571 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 178434465 | HCID 178434465 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09187473B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-ac673e267f554098af6775403731dde1 |
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| Source note | uspto-grants-2015_11 |
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