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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1749884Generated: November 2, 2026

Trifluoroacetic acid → HCID 178487226, compound

https://huagongshe.com/reaction/1749884

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 178487232HCID 178487232—
SolventDichloromethaneHCID 6344—
ProductHCID 178487226HCID 17848722644.9%

Reaction Steps

A solution of tert-butyl (Z)-4-({2-[(5-chloro-1H-indazol-3-yl)methylene]-6-methoxy-3-oxo-2,3-dihydrobenzofuran-7-yl}methyl)piperazine-1-carboxylate (0.0330 g, 0.0629 mmol) in methylene chloride (2 mL) was added with trifluoroacetic acid (2 mL) at room temperature, and the mixture was stirred overnight. The reaction mixture was concentrated, then the residue was added with saturated aqueous sodium hydrogencarbonate (10 mL), and the mixture was extracted three times with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate, and then the solvent was evaporated to obtain (Z)-2-[(5-chloro-1H-indazol-3-yl)methylene]-6-methoxy-7-(piperazin-1-ylmethyl)benzofuran-3(2H)-one (0.0120 g, 44%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156827B2
Source datasetuspto-grants-2015_10
ORD IDord-6fbc1d6b8a914b89b59fabdd13aa94aa
Source noteuspto-grants-2015_10