HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2401289Generated: October 30, 2026
Sodium Bicarbonate → HCID 86705195, compound
https://huagongshe.com/reaction/2401289
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Stannane, tributyl(1-ethoxyethenyl)- | HCID 619414 | — |
| Reactant | HCID 86705196 | HCID 86705196 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 86705195 | HCID 86705195 | 83% |
Reaction Steps
A suspension of N-(6-bromopyridin-3-yl)-2-{(5S)-5-(2-methylpropyl)-2-oxo-3-[6-(trifluoromethyl)pyridin-3-yl]imidazolidin-1-yl}acetamide (78 mg), tributyl(1-ethoxyvinyl)tin (145 mg), bis(triphenylphosphine)palladium(II) dichloride (22 mg), and copper(I) iodide (6.3 mg) in acetonitrile (1.5 mL) was stirred under irradiation with microwave at 150° C. for 2 hr. Saturated aqueous sodium hydrogen carbonate solution was added thereto, followed by extraction with chloroform. The organic layer was separated by phase separation cartridge, and the solvent was distilled off under reduced pressure. The residue was purified by preparative HPLC, 1M HCl (1.5 mL) was added to the resulting product, and the mixture was stirred at room temperature for 10 min. The mixture was made basic with saturated sodium hydrogen carbonate, followed by extraction with chloroform, and the solvent was distilled off under reduced pressure to afford the title compound (60 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08796272B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-38c068f38f4c43938f900e71348c5ea4 |
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| Source note | uspto-grants-2014_08 |
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