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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1373301Generated: October 30, 2026

Trifluoroacetic acid → HCID 135830908, compound

https://huagongshe.com/reaction/1373301

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 (r, 1H), 6.75 (m, 2H), 6.85 (s, 1H), 7.6 (d, 1H), 7.98 (s, 1H), 8.4 (s, H), 9.58 (s, 1H); Mass Spectrum: M+H+ 445 and 447.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07160891B2
Source datasetuspto-grants-2007_01
ORD IDord-289fe70af3cb44fc903f38251f35828b
Source noteuspto-grants-2007_01