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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1241581Generated: November 1, 2026

Trifluoroacetic acid → HCID 21936011, compound

https://huagongshe.com/reaction/1241581

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 21936081HCID 21936081—
SolventDichloromethaneHCID 6344—
ProductHCID 21936011HCID 2193601127.5%

Reaction Steps

A mixture of 7-[2-(N-tert-butoxycarbonyl-4-hydroxypiperidin-4-yl)ethoxy]-6-methoxy-4-(2,3-methylenedioxyanilino)quinazoline (0.067 g), trifluoroacetic acid (0.5 ml) and methylene chloride (3 ml) was stirred at ambient temperature for 1 hour. 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 brine, dried over magnesium sulphate and evaporated. There was thus obtained the title compound (0.015 g); NMR Spectrum: (DMSOd6 and CF3CO2D) 1.75 (m, 4H), 2.05 (t, 2H), 3.1 (m, 4H), 4.0 (s, 3H), 4.35 (t, 2H), 6.1 (s, 2H), 6.95 (m, 3H), 7.4 (s, 1H), 8.1 (s, 1H), 8.85 (s, 1H); Mass Spectrum: M+H+ 439.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115615B2
Source datasetuspto-grants-2006_10
ORD IDord-e1bf8993cd13445ea2642465b2a07f32
Source noteuspto-grants-2006_10