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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 451368Generated: October 30, 2026

Oxalyl chloride → HCID 58488524, compound

https://huagongshe.com/reaction/451368

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-(Methylsulfonyl)aniline hydrochlorideHCID 2735180—
ReactantHCID 58488523HCID 58488523—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58488524HCID 5848852484%

Reaction Steps

To a suspension of 5-(2-chloro-4-fluorophenyl)-4-methyl-1H-pyrrole-3-carboxylic acid (0.61 g, 2.4 mmol) in dichloromethane (30 ml) was added oxalyl chloride (0.41 ml, 4.8 mmol). The mixture was stirred at room temperature for 2.0 h, after which time the solvent was removed on a rotary evaporator. To this brown residue was added THF (40 ml), 4-(methanesulfonyl)aniline hydrochloride (495 mg, 2.38 mmol), and DIEA (1.6 ml, 9.5 mmol). The solution was stirred at room temperature for 20 h. The reaction mixture was concentrated on a rotary evaporator and 2N HCl (30 ml) was added to the residue. The solid was filtered and washed with 2N HCl, water and IPE to give the title compound (812 mg, 84%) as a brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08487117B2
Source datasetuspto-grants-2013_07
ORD IDord-d75ee2fec5bc4710bc546c922848871f
Source noteuspto-grants-2013_07