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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1826266Generated: November 2, 2026

Trifluoroacetic acid → HCID 22140839, compound

https://huagongshe.com/reaction/1826266

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 22140775HCID 22140775—
SolventDichloromethaneHCID 6344—
ProductHCID 22140839HCID 2214083993.1%

Reaction Steps

A mixture of 4-(2-bromo-5-methoxyanilino)-5-[N-(tert-butoxycarbonyl)piperidin-4-ylmethoxy]quinazoline (0.108 g), trifluoroacetic acid (1 ml) and methylene chloride (1 ml) was stirred at ambient temperature for 1.5 hours. The mixture was evaporated and the residue was triturated under diethyl ether. The resultant solid was isolated and dried under vacuum. The solid was dissolved in methylene chloride and few drops of a saturated methanolic ammonia solution was added. The solution was poured onto a chromatography column filled with silica and eluted with a 97:3 mixture of methylene chloride and a saturated methanolic ammonia solution. There was thus obtained the title compound (0.082 g); NMR Spectrum: (CDCl3) 1.2–1.4 (m, 2H), 1.9 (d, 2H), 2.3 (m, 1H), 2.65 (t, 2H), 3.12 (d, 2H), 3.84 (s, 3H), 4.2 (d, 2H), 6.61 (m, 1H), 6.93 (d, 1H), 7.5 (d, 2H), 7.68 (m, 1H), 8.22 (d, 1H), 8.68 (s, 1H); Mass Spectrum: M+H+ 443 and 445.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07049438B2
Source datasetuspto-grants-2006_05
ORD IDord-93e0955829594ccf9306ca65dcd24dff
Source noteuspto-grants-2006_05