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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2243573Generated: October 31, 2026

Trifluoroacetic acid → HCID 11635079, compound

https://huagongshe.com/reaction/2243573

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 58608123HCID 58608123—
SolventDichloromethaneHCID 6344—
ProductHCID 11635079HCID 11635079—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 4-(2-{2-[4-(2-morpholin-4-yl-ethoxy)-phenyl]-3-phenyl-furo[2,3-b]pyridin-4-ylamino}-ethyl)-piperazine-1-carboxylic acid tert-butyl ester 10d (0.062 g, 0.099 mmol) in dichloromethane (1.0 mL) was cooled to 0° C. Trifluoroacetic acid (0.5 mL) was added and the solution stirred under a nitrogen atmosphere at 0° C. for 15 min and then at room temperature for 2.5 h. The reaction mixture was concentrated and the residue was partitioned between ethyl acetate and saturated aqueous sodium bicarbonate solution. The organic phase was separated and washed with saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate, filtered and concentrated to afford 2-(4-((2-(4-morpholinyl)ethyl)oxy)phenyl)-3-phenyl-N-(2-(1-piperazinyl)ethyl)furo[2,3-b]pyridin-4-amine 10e as an off-white solid. MS (MH+) 528.3; Calculated 527 for C31H37N5O3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07674907B2
Source datasetuspto-grants-2010_03
ORD IDord-9f7ab69883954c83bdf603d9c0bbc8e2
Source noteuspto-grants-2010_03