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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 658939Generated: October 28, 2026

HCID 72323505, compound → HCID 72323504, compound

https://huagongshe.com/reaction/658939

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 72323505HCID 72323505—
ReactantHCID 86632081HCID 86632081—
SolventTolueneHCID 1140—
ProductHCID 72323504HCID 723235043.4%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of E/Z-6-chloro-3-[5-chloro-2-(1-methoxycarbonyl-1-methyl-ethoxy)-benzylidene]-2-oxo-2,3-dihydro-indole-1-carboxylic acid tert-butyl ester (1.5 g, 2.9 mmol) and 1-(4,5-difluoro-2-methyl-phenyl)-3-trimethylsilyoxy-2-aza-1,3-butadiene (13 mmol) in toluene (13 mL) was heated at 60° C. for 3 h, and concentrated in vacuo. To the residue was added DCM (30 mL) and TFA (5 mL), and the resultant solution was stirred at room temperature for 3 h, then concentrated in vacuo. The residue was partitioned between ethyl acetate and aqueous diluted NaOH solution. The organic layer was washed with water to neutral, dried over anhydrous Na2SO4, and concentrated. The residue was purified by flash chromatography to give the title compound as white solid (60 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08076482B2
Source datasetuspto-grants-2011_12
ORD IDord-bfd60cca93124d2899332fb1ab323783
Source noteuspto-grants-2011_12