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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2353743Generated: November 1, 2026

Sodium Carbonate → HCID 59379933, compound

https://huagongshe.com/reaction/2353743

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant4-(Tetramethyl-1,3,2-dioxaborolan-2-yl)anilineHCID 2734620—
ReactantHCID 59379971HCID 59379971—
CatalystHCID 178418476HCID 178418476—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 59379933HCID 5937993393.9%

Reaction Conditions

Temperature80 °C

Reaction Steps

Dichlorobis(triphenylphosphine)-palladium(II) (0.103 g, 0.15 mmol) was added to 2-chloro-4-[(3S)-3-methylmorpholin-4-yl]-6-(2-tert-butylsulfonylpropan-2-yl)pyrimidine (1.10 g, 2.93 mmol), 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline (0.833 g, 3.80 mmol) and 2M aqueous sodium carbonate (5.27 mL, 10.53 mmol) in DMF (6 mL), DME (5 mL), ethanol (5 mL) and water (12.5 mL) at RT under nitrogen. The reaction was purged with nitrogen for 15 minutes and the resulting mixture was stirred at 80° C. for 16 hours. The reaction mixture was diluted with ethyl acetate and washed with water. The organic solution was dried (MgSO4), filtered, and concentrated under reduced pressure. The residue was chromatographed on silica, eluting with 25%-100% ethyl acetate in isohexane, to give the desired material as a yellow solid (1.19 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07750003B2
Source datasetuspto-grants-2010_07
ORD IDord-7ec6242bfd264e0a9894382e308d779d
Source noteuspto-grants-2010_07