Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1615420Generated: October 29, 2026

Water → HCID 86680659, compound

https://huagongshe.com/reaction/1615420

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CarbonateHCID 10340—
Reactant4-(Isopropylsulphonyl)benzeneboronic acidHCID 44119327—
ReactantHCID 86680660HCID 86680660—
CatalystHCID 178418851HCID 178418851—
SolventAcetonitrileHCID 6342—
ProductHCID 86680659HCID 8668065988%

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of (4-isopropylsulfonylphenyl)boronic acid (892.7 mg, 3.914 mmol), tert-butyl (3R)-3-[4-[5-[3-[bis(tert-butoxycarbonyl)amino]-6-bromo-pyrazin-2-yl]isoxazol-3-yl]phenyl]morpholine-4-carboxylate (2.5 g, 3.558 mmol), Na2CO3 (3.558 mL of 2 M, 7.116 mmol), water (17.60 mL) and MeCN (25.00 mL) were degassed by vacuum/nitrogen cycles (3×) then Pd[P(tBu)3]2 (90.92 mg, 0.1779 mmol) was added and vessel flushed with nitrogen via vacuum/nitrogen cycles (2×). Mixture then heated at 50° C. (drysyn block temp) for 3 h. The reaction was cooled to rt, and then diluted with EtOAc (10 mL) and water (10 mL) and the organic layer separated and then washed with water (2×10 mL) and brine (1×10 mL), dried MgSO4, filtered and concentrated in vacuo. The crude product purified by ISCO (120 g SiO2, 0 to 50% EtOAc/petroleum ether) to leave product as a white foam (2.52 g, 88% yield)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765751B2
Source datasetuspto-grants-2014_07
ORD IDord-93fb027b28ea48c88a8e7064ddc59a06
Source noteuspto-grants-2014_07