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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384069Generated: October 30, 2026

Trifluoroacetic acid → HCID 178446248, compound

https://huagongshe.com/reaction/384069

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTriethylsilaneHCID 12052—
ReactantHCID 57969739HCID 57969739—
SolventDichloromethaneHCID 6344—
ProductHCID 178446248HCID 17844624875.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

tert-butyl 2-methyl-2-(3-(3-(trifluoromethyl)-1-trityl-1H-pyrazolo[3,4-b]pyridin-4-yl)phenyl)butylcarbamate (148 mg, 0.2142 mmol) was dissolved in dry DCM (2 mL) and cooled in an ice-bath. triethylsilane (99.63 mg, 136.9 μL, 0.8568 mmol) was added followed slowly dropwise by TFA (2 mL,). The resulting mixture was stirred at 0° C. for ˜1 hour 50 minutes. The reaction mixture was concentrated under reduced pressure to give a light brown solid/gum. This material was partitioned with ether and brine. The ether layer was washed with 1M HCl (2×10 mL) and the combined aqueous layer was basified with saturated NaHCO3 and extracted with EtOAc (3×10 mL). The combined EtOAc was dried over Na2SO4, filtered and concentrated under reduced pressure to give a colourless gum (56.5 mg). This material was purified by column chromatography (4.5% MeOH/0.5% NH4OH in DCM, ˜75 mL silica, loaded in DCM) to give a white powder (15 mg, 20% Yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367697B2
Source datasetuspto-grants-2013_02
ORD IDord-76d360991b8d4550b4f43b9c808a2989
Source noteuspto-grants-2013_02