Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1467314Generated: November 1, 2026

Trifluoroacetic acid → HCID 67996724, compound

https://huagongshe.com/reaction/1467314

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTriethylsilaneHCID 12052—
Reactant3-(2-methylpyridin-4-yl)-1-trityl-1H-indazole-5-carboxylic acidHCID 67984975—
SolventHydrochloric AcidHCID 313—
SolventDichloromethaneHCID 6344—
ProductHCID 67996724HCID 6799672485.2%

Reaction Conditions

Temperature23 °C

Reaction Steps

The synthetic intermediate from Step 1 (392 mg, 0.791 mmol), dichloromethane (2 ml), and trifluoroacetic acid (2 ml) were combined in an open vial. Triethylsilane (1.011 ml, 6.33 mmol) was then added, and the resulting mixture was stirred at a temperature of 23° C. for 50 minutes. The reaction mixture was then diluted with dichloromethane, and 2N HCl was added drop-wise until the pH of the mixture was between 4 and 5. This resulting precipitate was collected via filtration and rinsed with water, methanol and dichloromethane to afford 3-(2-methylpyridin-4-yl)-1H-indazole-5-carboxylic acid (220 mg, 0.674 mmol, 85% yield) as a green solid. The crude product was progressed to the next step without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08999957B2
Source datasetuspto-grants-2015_04
ORD IDord-ddc6a999266e45efb22620ed51efadd2
Source noteuspto-grants-2015_04