Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2099370Generated: October 31, 2026

Trifluoroacetic acid → HCID 67415388, compound

https://huagongshe.com/reaction/2099370

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 67415632HCID 67415632—
SolventDichloromethaneHCID 6344—
SolventTriethylsilaneHCID 12052—
ProductHCID 67415388HCID 67415388317.4%

Reaction Steps

Trifluoroacetic acid (50 ml) was added to a solution of tert-butyl 4-({4-[3-chloro-2-fluoroanilino]-6-methoxyquinazolin-7-yl}oxy)piperidine-1-carboxylate (750 mg, 1.49 mmol) in methylene chloride (1 ml) and triethylsilane (1 ml) and the solution stirred for 1 hour. The reaction mixture was then evaporated under reduced pressure and the residues re-dissolved in EtOAc (5 ml). This solution was then treated with 1M HCl/diethylether (1 ml) followed by more diethylether (50 ml) to give a white precipitate. The resulting solids were collected following centrifugation and dried under vacuum to give N-(3-chloro-2-fluorophenyl)-6-methoxy-7-(piperidin-4-yloxy)quinazolin-4-amine dihydrochloride as a white solid (750 mg); 1H NMR Spectrum: (DMSO-d6): 2.00-2.20 (m, 2H), 2.25-2.45 (m, 2H), 3.15-3.50 (m, 4H), 4.15 (s, 3H), 5.02 (m, 1H), 7.48 (m, 1H), 7.60-7.85 m, 3H), 8.35 (s, 1H), 8.85 (s, 1H), 9.56 (bs, 2H); Mass Spectrum: (M+H)+ 403.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07569577B2
Source datasetuspto-grants-2009_08
ORD IDord-7e24ec41221b4e199e02cd6411153a38
Source noteuspto-grants-2009_08