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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1241576Generated: October 30, 2026

Trifluoroacetic acid → HCID 21935994, compound

https://huagongshe.com/reaction/1241576

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 21936006HCID 21936006—
SolventDichloromethaneHCID 6344—
ProductHCID 21935994HCID 21935994225.8%

Reaction Steps

A mixture of 7-[3-(4-tert-butoxycarbonylpiperazin-1-yl)propoxy]-4-(6-chloro-2,3-methylenedioxyanilino)-6-methoxyquinazoline (0.286 g), trifluoroacetic acid (0.5 ml) and methylene chloride (6 ml) was stirred at ambient temperature for 3 hours. The solvent was evaporated and the residue was partitioned between methylene chloride and a saturated aqueous sodium bicarbonate solution. The organic phase was washed with water and with brine, dried over magnesium sulphate and evaporated. The material so obtained was triturated under a 6M solution of hydrogen chloride in diethyl ether. There was thus obtained the title compound (0.205 g); NMR Spectrum: (DMSOd6 and CF3CO2D) 2.35 (m, 2H), 3.2–3.9 (m, 10H), 4.0 (s, 3H), 4.35 (m, 2H), 6.12 (s, 2H), 7.0 (s, 1H), 7.1 (s, 1H), 7.38 (s, 1H), 8.15 (s, 1H), 8.85 (s, 1H); Mass Spectrum: M+H+ 472 and 474

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115615B2
Source datasetuspto-grants-2006_10
ORD IDord-9a1ed4f174a24ab6a22838a73bf05f69
Source noteuspto-grants-2006_10