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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 500269Generated: October 26, 2026

Methylamine → Benzenesulfonamide, 4-(2-amino-5-pyrimidinyl)-2-fluoro-N-methyl-

https://huagongshe.com/reaction/500269

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
ReactantTriethylamineHCID 8471—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Bromo-2-fluorobenzene-1-sulfonyl chlorideHCID 2736310—
Reactant2-Aminopyrimidine-5-boronic acid, pinacol esterHCID 17750212—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
ProductBenzenesulfonamide, 4-(2-amino-5-pyrimidinyl)-2-fluoro-N-methyl-HCID 6722516984.6%

Reaction Steps

4-Bromo-2-fluorobenzenesulfonyl chloride (100 mg, 0.36 mmol) was added to a mixture of methylamine (2M in THF, 0.275 mL, 0.55 mmol) and triethylamine (0.10 mL, 0.73 mmol) in methylene chloride (2.0 mL). The reaction mixture was quenched with saturated NaHCO3 (1.0 mL) and concentrated to afford the crude intermediate in water. A mixture of the intermediate in water, 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrimidin-2-amine (81 mg, 0.36 mmol), tetrakis(triphenylphosphine)palladium (20 mg, 0.02 mmol), potassium carbonate (150 mg, 1.1 mmol) in toluene (2.0 mL) and ethanol (1.0 mL) was heated at 110° C. for 2 h. After cooling to RT, ether was added to the mixture and the solid was filtered, washed with water and ether to afford the desired product (0.086 g, 83%). LCMS: (M+H)=282.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07767675B2
Source datasetuspto-grants-2010_08
ORD IDord-4fadf6f84e47405cb4b56c44ff8d3ccb
Source noteuspto-grants-2010_08