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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 890971Generated: October 29, 2026

Trifluoroacetic acid → HCID 178486732, compound

https://huagongshe.com/reaction/890971

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 178486731HCID 178486731—
SolventDichloromethaneHCID 6344—
ProductHCID 178486732HCID 17848673262.1%

Reaction Steps

A mixture of N-(2-tert-butoxycarbonylaminoethyl)-N′-(2,6-dimethylphenyl)-N″-[6-methoxy-7-(N-methylpiperidin-4-ylmethoxy)quinazolin-4-yl]guanidine (0.31 g), trifluoroacetic acid (1 ml) and methylene chloride (1 ml), was stirred at ambient temperature for 20 minutes. The reaction mixture was evaporated and the residue was dissolved in water (4 ml) and the solution was basified to pH10 by the addition of 10N aqueous potassium hydroxide solution. The mixture was extracted with a 19:1 mixture of methylene chloride and methanol. The organic extract was dried over magnesium sulphate and evaporated. There was thus obtained the title compound (0.16 g); NMR Spectrum: (DMSOd6) 1.2–1.4 (m, 2H), 1.65–1.94 (m, 5H),2.12 (s, 3H), 2.21 (s, 6H), 2.7–2.9 (m, 4H), 3.22 (br s, 3H), 3.4–3.8 (m, 4H), 3.91 (d, 2H), 7.0 (s, 1H), 7.13 (s, 3H), 8.4 (s, 1H); Mass Spectrum: M+H+ 492.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07001904B1
Source datasetuspto-grants-2006_02
ORD IDord-2b393a6587f7495c86cd42c285e2f740
Source noteuspto-grants-2006_02