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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 509600Generated: November 4, 2026

Hydrochloric Acid → 5-Methanesulfonyl-pyridine-2-carboxylic acid (2-chloro-4-trifluoromethoxy-phenyl)-amide

https://huagongshe.com/reaction/509600

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-Chloro-4-(trifluoromethoxy)anilineHCID 2734084—
ReactantTrimethylaluminumHCID 16682925—
ReactantMethyl 5-(methylsulfonyl)picolinateHCID 53429647—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
Product5-Methanesulfonyl-pyridine-2-carboxylic acid (2-chloro-4-trifluoromethoxy-phenyl)-amideHCID 86709640—

Reaction Conditions

Temperature85 °C

Reaction Steps

2-Chloro-4-trifluoromethoxy-phenylamine (2.0 g, 9.29 mmol) in toluene (50 mL) was added to trimethylaluminum (2.0 M 4.65 mL) then methyl 5-(methylsulfonyl)picolinate 6 (1.0 g, 4.65 mol) was added and the mixture was heated to 80-90° C. for 2 h. The reaction was cooled down and 1N HCl solution (10 mL) was added to be acidic. Dichloromethane (100 mL) was then added and the organic phase was further washed with water (100 mL) and dried over sodium sulfate. The solvent was removed and the residue was mixed with ether (50 mL) and stirred for 0.5 h. The solid was filtered and dried to give 5-methanesulfonyl-pyridine-2-carboxylic acid (2-chloro-4-trifluoromethoxy-phenyl)-amide 7 as a light yellow solid. Yield: 1.26 g, 65%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096587B2
Source datasetuspto-grants-2015_08
ORD IDord-675cde833926421d9058a65d12f4f376
Source noteuspto-grants-2015_08