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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2353747Generated: November 2, 2026

Sodium Carbonate → HCID 59380104, compound

https://huagongshe.com/reaction/2353747

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant4-(Tetramethyl-1,3,2-dioxaborolan-2-yl)anilineHCID 2734620—
ReactantHCID 59380049HCID 59380049—
CatalystHCID 178418476HCID 178418476—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventEthyl AcetateHCID 8857—
ProductHCID 59380104HCID 5938010494.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

A stream of nitrogen was passed through a mixture of 2-chloro-4-[2-(3,5-difluorophenyl)sulfonylpropan-2-yl]-6-[(3S)-3-methylmorpholin-4-yl]pyrimidine (1.4 g, 3.24 mmol), 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline (0.923 g, 4.21 mmol) and 2M aqueous sodium carbonate (5.83 mL, 11.67 mmol) in DMF (6 mL), DME (5 mL), ethanol (5 mL) and water (12.5 mL) at RT. The reaction mixture was treated with dichlorobis(triphenylphosphine)palladium(II) (0.114 g, 0.16 mmol) and was stirred at 80° C. for 1 hour. The reaction mixture was diluted with ethyl acetate and washed with water. The organic solution was dried (MgSO4) and concentrated under reduced pressure. The residue was chromatographed on silica, eluting with 25%-60% ethyl acetate in isohexane, to give the desired material as a pale yellow solid (1.496 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07750003B2
Source datasetuspto-grants-2010_07
ORD IDord-4742ef5a556e412ab2b778db71941afd
Source noteuspto-grants-2010_07