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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22781Generated: October 30, 2026

Trifluoroacetic acid → HCID 22591472, compound

https://huagongshe.com/reaction/22781

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 22591455HCID 22591455—
SolventDichloromethaneHCID 6344—
ProductHCID 22591472HCID 2259147259.9%

Reaction Steps

A mixture of 7-(N-tert-butoxycarbonylpiperidin-4-ylmethoxy)-4-(6-chlorobenzofuran-7-ylamino)-6-methoxyquinazoline (0.4 g), trifluoroacetic acid (3 ml) and methylene chloride (12 ml) was stirred at ambient temperature for 3 hours. The mixture was evaporated and the residue was diluted with water. The mixture was basified to pH11 by the addition of 1 N aqueous sodium hydroxide solution and methylene chloride was added. The precipitate which was formed was collected by filtration, washed with water and dried under vacuum to give the title compound (0.195 g); NMR Spectrum: (DMSOd6 and CF3CO2D) 1.55 (m, 2H), 2.0 (m, 2H), 2.25 (m, 1H), 2.95 (m, 2H), 3.4 (m, 2H), 4.05 (s, 3H), 4.2 (d, 2H), 7.1 (d, 1H), 7.4 (s, 1H), 7.55 (d, 1H), 7.8 (d, 1H), 8.05 (d, 1H), 8.2 (s, 1H), 8.85 (s, 1H), Mass Spectrum: M−H− 437.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06849625B2
Source datasetuspto-grants-2005_02
ORD IDord-4ba40502caba4ec296e1b49588043d09
Source noteuspto-grants-2005_02