HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 658939Generated: October 28, 2026
HCID 72323505, compound → HCID 72323504, compound
https://huagongshe.com/reaction/658939
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 72323505 | HCID 72323505 | — |
| Reactant | HCID 86632081 | HCID 86632081 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 72323504 | HCID 72323504 | 3.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08076482B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-bfd60cca93124d2899332fb1ab323783 |
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| Source note | uspto-grants-2011_12 |
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