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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 641726Generated: October 31, 2026

Trifluoroacetic acid → HCID 22140839, compound

https://huagongshe.com/reaction/641726

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 numberUS07696214B2
Source datasetuspto-grants-2010_04
ORD IDord-ba366ef3d6024d83a028f55a41b6c0ea
Source noteuspto-grants-2010_04