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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1983473Generated: October 25, 2026

Trifluoroacetic acid → [3-(3-Fluorophenyl)-1H-5-indazolyl]methanamine

https://huagongshe.com/reaction/1983473

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant1h-Indazole-1-carboxylic acid,5-(aminomethyl)-3-(3-fluorophenyl)-,1,1-dimethylethyl esterHCID 22260694—
SolventDichloromethaneHCID 6344—
Product[3-(3-Fluorophenyl)-1H-5-indazolyl]methanamineHCID 2226072888.7%

Reaction Steps

To a solution of 300 mg of tert-butyl 5-(aminomethyl)-3-(3-fluorophenyl)-1H-1-indazolecarboxylate in 1 ml methylene chloride was added 2 ml of trifluoroacetic acid, and the mixture was stirred at room temperature for 6.5 hours. After removing the solvent by filtration, to the residue was added 20 ml of ethyl acetate. The mixture was sequentially washed with saturated aqueous sodium hydrogencarbonate solution (×2) and brine, dried over anhydrous magnesium sulfate and the solvent was evaporated, to give 188 mg of the title compound as yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07541376B2
Source datasetuspto-grants-2009_06
ORD IDord-623963d954384d128b466199a06003b7
Source noteuspto-grants-2009_06