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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2249517Generated: November 2, 2026

Hydrochloric Acid → 4-(2,3-Difluoro-phenylcarbamoyl)-1-methanesulfonyl-1H-pyrrole-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/2249517

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant2,3-DifluoroanilineHCID 78278—
Reactant1-Methanesulfonyl-1H-pyrrole-2,4-dicarboxylic acid 2-methyl esterHCID 58685819—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product4-(2,3-Difluoro-phenylcarbamoyl)-1-methanesulfonyl-1H-pyrrole-2-carboxylic acid methyl esterHCID 5868582198%

Reaction Steps

To a solution of 1-methanesulfonyl-1H-pyrrole-2,4-dicarboxylic acid 2-methyl ester (290 mg, 1.17 mmol) in dry CH2Cl2 (5 mL) and DMF (2 drops) was added oxalyl chloride (220 mg, 1.73 mmol) at room temperature. The mixture was stirred for 1 hour and evaporated. The residue was dried on the vacuum pump for 4 hours and then dissolved in dry CH2Cl2 (5 mL). To this solution was added 2,3-difluoro-phenylamine (300 mg, 2.32 mmol) and triethylamine (240 mg, 2.37 mmol). The reaction mixture was stirred for another 1 hour then poured into 2N HCl solution. The aqueous solution was extracted with EtOAc and the combined organic layers were dried over MgSO4. After removal of solvent by evaporation, the residue was purified by flash column eluting with 20% EtOAc/hexanes to afford the title compound as a yellow solid (410 mg, 98%). MS (ES+): m/e=359.1 (M+H); LC/Method A/3.31 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07314885B2
Source datasetuspto-grants-2008_01
ORD IDord-de6887101c8b4e6d9b5dcfd7d00d680c
Source noteuspto-grants-2008_01