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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 729623Generated: October 29, 2026

Trifluoroacetic acid → HCID 57832821, compound

https://huagongshe.com/reaction/729623

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 69056157HCID 69056157—
SolventDichloromethaneHCID 6344—
ProductHCID 57832821HCID 57832821—

Reaction Conditions

Temperature22 °C

Reaction Steps

To a cold solution of 4-{4-[3-(5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl)-ureido]-isoquinolin-1-yloxy}-piperidine-1-carboxylic acid tert-butyl ester (820 mg, 1.37 mmol) in dichloromethane (50 mL), add trifluoroacetic acid (15 mL). Stir the reaction mixture at 22° C. for 1.5 hours. After removal of solvent, treat the residue with 1N sodium hydroxide saturated with NaCl (50 mL) and extract five times with dichloromethane (50 mL each). Dry the combined organic phases over sodium sulfate. Filter the mixture and subject residue to silica gel chromatography eluting with dichloromethane and methanol to provide a white solid (515 mg, 75% yield, LCMS ES+ (m/z) 499.5 [M+H]).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582638B2
Source datasetuspto-grants-2009_09
ORD IDord-259722e5a8b04e7f9be62e2e3aa9cf93
Source noteuspto-grants-2009_09