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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 227221Generated: October 30, 2026

Trifluoroacetic acid → HCID 10367176, compound

https://huagongshe.com/reaction/227221

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 11657016HCID 11657016—
SolventDichloromethaneHCID 6344—
ProductHCID 10367176HCID 10367176—

Reaction Conditions

Temperature30 °C

Reaction Steps

213 mg of 1-[(benzyloxycarbonyl)methyl]-3-methyl-7-(2-butyn-1-yl)-8-[(R)-3-(tert.-butyloxycarbonylamino)-piperidin-1-yl]-xanthine in 2 ml methylene chloride are combined with 1 ml of trifluoroacetic acid and the reaction mixture is shaken for 20 minutes at 30° C. For working up it is made alkaline with 15 ml of 1 N sodium hydroxide solution and the organic phase is separated off. The aqueous phase is extracted with methylene chloride and the combined organic phases are evaporated down. The flask residue is purified through a silica gel column with methylene chloride/methanol (100:0 to 70:30) as eluant.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560450B2
Source datasetuspto-grants-2009_07
ORD IDord-c56b1f38c5d74fbf89f8811bcbd08d5f
Source noteuspto-grants-2009_07