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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 922984Generated: October 30, 2026

Isobutyl iodide → methyl 2-chloro-4-(N-isobutylmethylsulfonamido)benzoate

https://huagongshe.com/reaction/922984

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsobutyl iodideHCID 10556—
ReactantCesium carbonateHCID 10796—
ReactantMethyl 2-chloro-4-(methylsulfonamido)benzoateHCID 54238017—
SolventDimethylformamideHCID 6228—
Productmethyl 2-chloro-4-(N-isobutylmethylsulfonamido)benzoateHCID 66877616—

Reaction Conditions

Temperature140 °C

Reaction Steps

175 μL of 1-iodo-2-methylpropane and 740 mg of Cesium Carbonate were added to 200 mg of methyl 2-chloro-4-(methylsulfonamido)benzoate in 2 mL of DMF and stirred in the microwave at 140° C. for 30 minutes. The reaction mixture was extracted in Ethyl Acetate twice with water, dried over Magnesium Sulfate, filtered, concentrated and purified on ISCO Combi-Flash to give methyl 2-chloro-4-(N-isobutylmethylsulfonamido)benzoate. 120 mg of methyl 2-chloro-4-(N-isobutylmethylsulfonamido)benzoate was hydrolyzed via Procedure M to yield 110 mg of crude 2-chloro-4-(N-isobutylmethylsulfonamido)benzoic acid. 75 mg of 4-chloro-3-(pyridin-2-yl)aniline was coupled to 2-chloro-4-(N-isobutylmethylsulfonamido)benzoic acid via Procedure G. The crude product was purified by reverse phase HPLC to yield 2-chloro-N-(4-chloro-3-(pyridin-2-yl)phenyl)-4-(N-isobutylmethylsulfonamido)benzamide. MS (Q1) 492 (M)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278961B2
Source datasetuspto-grants-2016_03
ORD IDord-c13be81b901149cb8ddd5f4d229f6547
Source noteuspto-grants-2016_03