HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 572849Generated: October 29, 2026
Potassium Carbonate → HCID 66835664, compound
https://huagongshe.com/reaction/572849
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Dicyclohexylphosphino-2',6'-diisopropoxybiphenyl | HCID 16217985 | — |
| Reactant | Potassium (3-tert-butoxy-3-oxopropyl)(trifluoro)borate(1-) | HCID 49761675 | — |
| Reactant | HCID 66835733 | HCID 66835733 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 66835664 | HCID 66835664 | — |
Reaction Steps
A screw-cap tube is charged with 2-[(3-bromophenyl)(1-methylpiperidin-4-yloxy)methyl]benzothiazole (208 mg), palladium(II) acetate (3 mg), RuPhos® (12 mg), potassium 3-trifluoroboratopropionate tert-butyl ester (118 mg), potassium carbonate (207 mg), water (2.5 mL) and toluene (2.5 mL). The tube is evacuated, filled with argon and sealed. After stirring at 120° C. overnight, the mixture is diluted with ethyl acetate and water and the aqueous phase is extracted with ethyl acetate. The pooled organic extracts are dried over magnesium sulfate and concentrated under reduced pressure. The residue is purified by chromatography (gradient dichloromethane/methanol from 100/0 to 95/5) to afford 3-{3-[benzothiazol-2-yl(1-methylpiperidin-4-yloxy)methyl]phenyl}propionic acid tert-butyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09029357B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-d95913f7b4f1458ab1e576033e534949 |
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| Source note | uspto-grants-2015_05 |
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