HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2277304Generated: October 31, 2026
Cesium carbonate → tert-butyl (6-(((2S)-2-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)propyl)oxy)-5-fluoropyridin-3-yl)carbamate
https://huagongshe.com/reaction/2277304
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | tert-Butyl carbamate | HCID 77922 | — |
| Reactant | 1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine) | HCID 636044 | — |
| Reactant | HCID 86731385 | HCID 86731385 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | tert-butyl (6-(((2S)-2-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)propyl)oxy)-5-fluoropyridin-3-yl)carbamate | HCID 86731386 | 47.7% |
Reaction Steps
A mixture of 2-((2S)-1-((5-bromo-3-fluoropyridin-2-yl)oxy)propan-2-yl)-1H-isoindole-1,3(2H)-dione (3.10 g), tert-butyl carbamate (0.958 g), tris(dibenzylideneacetone)dipalladium(0) (0.374 g), 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (0.710 g), cesium carbonate (5.33 g) and toluene (30 mL) was stirred at 110° C. overnight under an argon atmosphere. To the reaction mixture was added water, and the mixture was extracted with ethyl acetate. The combined organic layer were washed with saturated brine, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (1.62 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09133129B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-464fa5ce160b417899661593bdb2f18e |
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| Source note | uspto-grants-2015_09 |
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