HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 633843Generated: October 31, 2026
Cesium carbonate → HCID 178487796, compound
https://huagongshe.com/reaction/633843
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | (1,1'-Binaphthalen)-2-yldi-tert-butylphosphine | HCID 2734941 | — |
| Reactant | HCID 178487874 | HCID 178487874 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 178487796 | HCID 178487796 | 67% |
Reaction Steps
Cesium carbonate (3.1 g, 9.46 mmol, 2.0 eq) is added at room temperature to a stirred solution of {trans-4-[3-(3-chloro-6-methoxy-quinolin-4-yl)-1,2-dihydroxy-propyl]-cyclohexyl}-carbamic acid tert-butyl ester (2.2 g, 4.73 mmol, 1.0 eq) in dioxane (70 mL), followed by palladium(II) acetate (159 mg, 0.71 mmol, 0.15 eq) and racemic-2-di-tert-butylphosphino-1,1′-binaphthyl (283 mg, 0.71 mmol, 0.15 eq). After 3 hours stirring at 100° C., solvent is removed and the residue is extracted with dichloromethane (3×100 mL) and water (100 mL). The combined organic layers are washed with brine, dried over sodium sulfate, filtered and concentrated to afford {trans-4-[hydroxy-(8-methoxy-1,2-dihydro-furo[2,3-c]quinolin-2-yl)-methyl]-cyclohexyl}-carbamic acid tert-butyl ester as a light grey solid (1.35 g, 67% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09321788B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-6f53f808efdc4fd29850c16ab40ce674 |
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| Source note | uspto-grants-2016_04 |
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