Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850680Generated: November 2, 2026

Trifluoroacetic acid → HCID 90411374, compound

https://huagongshe.com/reaction/1850680

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 131732451HCID 131732451—
SolventDichloromethaneHCID 6344—
ProductHCID 90411374HCID 9041137498%

Reaction Steps

To a suspension of tert-butyl 1-[4-[(2-amino-6-fluoro-pyrazolo[1,5-a]pyrimidine-3-carbonyl)amino]-3-pyridyl]piperidine-4-carboxylate trifluoroacetic acetate (prepared according to a methodology similar to the one described in Example 1) (101 mg, 0.1773 mmol) in DCM (5 mL) was added TFA (1 mL, 12.98 mmol). The mixture was stirred at room temperature for 20 hours. The solvent was removed in vacuo and the residue azeotroped with DCM (×2) and diethyl ether (×2) to give title compound as a beige solid (98% Yield, di-TFA salt). 1H NMR (500 MHz, DMSO) δ 11.10 (s, 1H), 9.58 (dd, 1H), 8.91 (d, 1H), 8.86 (d, 1H), 8.68 (s, 1H), 8.56 (d, 1H), 6.92 (s, 2H), 3.10 (d, 2H), 2.99-2.82 (m, 2H), 2.53-2.50 (m, 1H), 2.15-1.93 (m, 4H); 19F NMR (471 MHz, DMSO) δ −74.10, −151.83; LC-MS ES+: 400.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957078B2
Source datasetuspto-grants-2015_02
ORD IDord-f85a41b2c803401c8e42fcf3e1b089c8
Source noteuspto-grants-2015_02