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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 499060Generated: October 26, 2026

Sodium Iodide → 2-Chloro-N-{4-[4-chloro-6-(5-methyl-2H-pyrazol-3-ylamino)-pyrimidin-2-ylsulfanyl]-phenyl)-benzamide

https://huagongshe.com/reaction/499060

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Chloro-N-(4-(4,6-dichloropyrimidin-2-ylthio)phenyl)benzamideHCID 59420797—
ReactantHCID 178418690HCID 178418690—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-Chloro-N-{4-[4-chloro-6-(5-methyl-2H-pyrazol-3-ylamino)-pyrimidin-2-ylsulfanyl]-phenyl)-benzamideHCID 17842822582.1%

Reaction Conditions

Temperature90 °C

Reaction Steps

A 250 mL round bottom flask was charged with 2-chloro-N-[4-(4,6-dichloro-pyrimidin-2-ylsulfanyl)-phenyl]-benzamide (12.5 g, 30.4 mmol), 5-methyl-2H-pyrazol-3-ylamine (3.55 g, 36.5 mmol), sodium iodide (4.56 g, 30.4 mmol), N,N-diisopropylethylamine (6.9 mL, 40.0 mmol) and N,N-dimethylformamide (125 mL) under nitrogen. The reaction mixture was stirred at 90° C. for 5 h, then allowed to cool to room temperature. Water (600 mL) was added and the resulting suspension stirred at room temperature for 2 h and the solid collected by filtration and dried. The resulting white solid was triturated with hot ethyl acetate (50 mL), filtered and washed with ethyl acetate (1×20 mL) to give the title compound as a white solid (11.76 g, 82 %). 1H NMR (DMSO): 2.16 (3H, s), 5.30 (1H, s), 6.48 (1H, s), 7.49-7.62 (6H, m), 7.89 (2H, m), 10.28 (1H, s), 10.84 (1H, s), 11.93 (1H, s); MS (ES+): 471.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07767672B2
Source datasetuspto-grants-2010_08
ORD IDord-e7b46fa718e14833817e3138bc8dfcb8
Source noteuspto-grants-2010_08