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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1241583Generated: October 30, 2026

Trifluoroacetic acid → HCID 21935985, compound

https://huagongshe.com/reaction/1241583

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 21936076HCID 21936076—
ProductHCID 21935985HCID 21935985—

Reaction Steps

Using an analogous procedure to that described in Example 11, 7-(N-tert-butoxycarbonylpiperidin-4-ylmethoxy)-4-(6-chloro-2,3-methylenedioxyanilino)-6-methoxyquinazoline was reacted with trifluoroacetic acid. The material so obtained was triturated under a 6M solution of hydrogen chloride in diethyl ether. There was thus obtained the title compound; NMR Spectrum: (DMSOd6) 1.5–1.65 (m, 2H), 2.0 (d, 2H), 2.2 (m, 1H), 2.95 (m, 2H), 3.2–3.4 (m, 2H), 4.02 (s, 3H), 4.12 (d, 2H), 6.15 (s, 2H), 7.05 (d, 1H), 7.15 (d, 1H), 7.42 (s, 1H), 8.22 (s, 1H), 8.8 (s, 1H); Mass Spectrum: M+H+ 443 and 445.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115615B2
Source datasetuspto-grants-2006_10
ORD IDord-67e4e225f0084ed88996b9b4740655ee
Source noteuspto-grants-2006_10