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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 641750Generated: October 30, 2026

Trifluoroacetic acid → HCID 135830908, compound

https://huagongshe.com/reaction/641750

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 10165579HCID 10165579—
ProductHCID 135830908HCID 135830908—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 7-benzyloxy-4-(2-bromo-5-methoxyanilino)-5-piperidin-4-yloxyquinazoline (0.35 g) and trifluoroacetic acid (6 ml) was stirred and heated to 80° C. for 5 hours. The mixture was evaporated and the residue was dissolved in water (12 ml). The solution was basified to pH8 by the addition of sodium bicarbonate. The resultant precipitate was isolated, washed with water and with ethyl acetate and dried under vacuum. There was thus obtained the title compound (0.26 g); NMR Spectrum: (DMSOd6) 1.95-2.15 (m, 2H), 2.32 (d, 2H), 3.05 (t, 2H), 3.3-3.4 (m, 2H), 3.8 (s, 3H), 5.0 (m, 1H), 6.75 (m, 2H), 6.85 (s, 1H), 7.6 (d, 1H), 7.98 (s, 1H), 8.4 (s, 1H), 9.58 (s, 1H); Mass Spectrum: M+H+ 445 and 447.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07696214B2
Source datasetuspto-grants-2010_04
ORD IDord-2ee109c9477a4e059474dbcc2179581b
Source noteuspto-grants-2010_04