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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2217269Generated: November 3, 2026

Trifluoroacetic acid → HCID 17958697, compound

https://huagongshe.com/reaction/2217269

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 17958696HCID 17958696—
SolventDichloromethaneHCID 6344—
ProductHCID 17958697HCID 17958697—

Reaction Conditions

Temperature40 °C

Reaction Steps

2 mL of trifluoroacetic acid were added to the ice-cooled solution of 1.1 g (2.561 mmol) of 3,4-dihydro-3-[1-(1,1-dimethylethoxycarbonyl)-4-piperidinyl]-6-(4-methyl-1-piperazinyl)-2(1H)-quinazolinone in 20 mL of methylene chloride. The reaction mixture was stirred for 15 hours at ambient temperature and for 5 hours at 40° C. and then evaporated down in vacuo. The residue remaining was taken up in 5 mL of water, the solution formed was saturated with potassium carbonate and extracted exhaustively with dichloromethane. The combined extracts were evaporated down in vacuo. The residue obtained was purified by column chromatography on silica gel using dichloromethane/methanol 9/1 (v/v) to start with, then dichloromethane/methanol/concentrated ammonia 70/30/3 (v/v/v) as eluant. The appropriate fractions were evaporated down in vacuo, the residue remaining (0.5 g; 59% of theoretical) was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07407963B2
Source datasetuspto-grants-2008_08
ORD IDord-00f03940d88d4d19903f8bc62e802cc8
Source noteuspto-grants-2008_08