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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 509536Generated: November 3, 2026

Sodium Carbonate → HCID 67480518, compound

https://huagongshe.com/reaction/509536

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant4,4,5,5-Tetramethyl-2-[4-(propane-2-sulfonyl)phenyl]-1,3,2-dioxaborolaneHCID 53217101—
ReactantHCID 67481718HCID 67481718—
CatalystHCID 178418476HCID 178418476—
SolventDimethylformamideHCID 6228—
SolventWater ethylacetateHCID 22728543—
ProductHCID 67480518HCID 6748051898%

Reaction Conditions

Temperature80 °C

Reaction Steps

tert-Butyl N-[[4-[5-[2-[bis(tert-butoxycarbonyl)amino]-5-bromo-3-pyridyl]-1,3,4-oxadiazol-2-yl]phenyl]methyl]-N-methyl-carbamate (120 mg, 0.1817 mmol) was dissolved in DMF (1.2 mL) and 2-(4-isopropylsulfonylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (84.57 mg, 0.2726 mmol) and Pd(PPh3)2Cl2 (7.516 mg, 0.01817 mmol) were added. 2M aqueous Na2CO3 (272.6 μL, 0.5451 mmol) was added and the reaction heated at 80° C. for 1 hour in a sealed tube. The reaction mixture was cooled to ambient temperature and diluted with EtOAc/water. The layers were separated and the aqueous layer extracted with EtOAc (×2). The combined organic extracts were washed with water (×3), brine (×2), dried (MgSO4), filtered and concentrated in vacuo. The resultant residue was purified by column chromatography (ISCO Companion™, 4 g column, 0-50% EtOAc/Petroleum ether) to give the impure sub-title compound as a yellow oil (136 mg). This was used directly in the next step with no further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096584B2
Source datasetuspto-grants-2015_08
ORD IDord-5dda399ee2c549c2b7cb5dc3888992a6
Source noteuspto-grants-2015_08