Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595265Generated: October 29, 2026

Trifluoroacetic acid → HCID 72706748, compound

https://huagongshe.com/reaction/595265

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 131734580HCID 131734580—
SolventDichloromethaneHCID 6344—
ProductHCID 72706748HCID 72706748—

Reaction Steps

TFA (24 μL, 0.31 mmol) was added to a solution of N-{3-[1-(2-{[tert-butyl(dimethyl)silyl]-oxy}ethyl)-1H-pyrazol-4-yl]-5-methylphenyl}-4-(trifluoromethyl)pyrimidin-2-amine in dichloromethane (2 mL), and the reaction was allowed to stir for 30 minutes. The competed reaction was concentrated under reduced pressure. The residue was purified by reverse phase HPLC (ACN/water with 0.1% formic acid modifier to afford 2-[4-(3-methyl-5-{[4-(trifluoromethyl)pyrimidin-2-yl]amino}phenyl)-1H-pyrazol-1-yl]ethanol. MS ESI calcd. for C17H17F3N5O [M+H]+ 364. found 364. 1H NMR (500 MHz, DMSO-d6) δ 10.10 (s, 1H), 8.79 (d, J=4.9, 1H), 8.00 (s, 1H), 7.81 (s, 1H), 7.73 (s, 1H), 7.31 (s, 1H), 7.23 (d, J=4.9, 1H), 7.05 (s, 1H), 4.92 (t, J=5.2, 1H), 4.14 (t, J=5.6, 2H), 3.73 (q, J=5.6, 2H), 2.27 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242984B2
Source datasetuspto-grants-2016_01
ORD IDord-7343f29416a44645af111a9ac1817964
Source noteuspto-grants-2016_01