Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2068425Generated: November 1, 2026

Trifluoroacetic acid → Methyl 5-[4-fluoro-2-(4-fluorophenyl)-3-[(methylamino)carbonyl]pyrazolo[1,5-a]pyridin-5-yl]-2-methoxy-6-methyl-3-pyridinecarboxylate

https://huagongshe.com/reaction/2068425

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 59411413HCID 59411413—
SolventDichloromethaneHCID 6344—
ProductMethyl 5-[4-fluoro-2-(4-fluorophenyl)-3-[(methylamino)carbonyl]pyrazolo[1,5-a]pyridin-5-yl]-2-methoxy-6-methyl-3-pyridinecarboxylateHCID 59411422—

Reaction Steps

To a solution containing methyl 5-(3-(tert-butoxycarbonyl(methyl)carbamoyl)-4-fluoro-2-(4-fluorophenyl)pyrazolo[1,5-a]pyridin-5-yl)-2-methoxy-6-methylnicotinate (0.07 g, 0.13 mmol) and dichloromethane (2.5 mL) was added TFA (0.39 mL, 5.0 mmol) at room temperature. The solution was maintained for 15 minutes and concentrated to dryness to afford Methyl 5-(4-fluoro-2-(4-fluorophenyl)-3-(methylcarbamoyl)pyrazolo[1,5-a]pyridin-5-yl)-2-methoxy-6-methylnicotinate as a tan solid which was used without further purification. LCMS retention time: 1.777 min. LC data was recorded on a Shimadzu LC-10AS liquid chromatograph equipped with a Phenomenex-Luna, 10 micron, C18, 3.0×50 mm column using a SPD-10AV UV-Vis detector at a detector wave length of 220 nM. The elution conditions employed a flow rate of 4 mL/min, a gradient of 100% solvent A/0% solvent B to 0% solvent A/100% solvent B, a gradient time of 3 min, a hold time of 1 min, and an analysis time of 4 min where solvent A was 10% methanol/90% H2O/10 mM TFA and solvent B was 10% H2O/90% methanol/10 mM TFA. MS data was determined using a Micromass Platform for LC in electrospray mode. m/z 489 (MNa+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08293909B2
Source datasetuspto-grants-2012_10
ORD IDord-f2b3405d38844477925740a31a68c95b
Source noteuspto-grants-2012_10