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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1715102Generated: November 2, 2026

Water → 4-[2-(2,4-dichlorophenyl)-5-methyl-4-[(piperidin-1-ylamino)carbonyl]-1H-imidazol-1-yl]phenyl thiophene-2-sulfonate

https://huagongshe.com/reaction/1715102

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant2-Thiophenesulfonyl chlorideHCID 85518—
Reactant2-(2,4-Dichlorophenyl)-1-(4-hydroxyphenyl)-5-methyl-1H-imidazole-4-carboxylic acid piperidin-1-ylamideHCID 58965075—
SolventDichloromethaneHCID 6344—
Product4-[2-(2,4-dichlorophenyl)-5-methyl-4-[(piperidin-1-ylamino)carbonyl]-1H-imidazol-1-yl]phenyl thiophene-2-sulfonateHCID 1150527483%

Reaction Conditions

Temperature-78 °C

Reaction Steps

2-(2,4-Dichlorophenyl)-1-(4-hydroxyphenyl)-5-methyl-N-piperidin-1-yl-1H-imidazole-4-carboxamide, prepared as described in Ex. 2, Step 1 (100 mg, 0.22 mmol) and triethylamine (0.31 ml, 2.25 mmol) in dichloromethane (2.5 ml) were cooled to −78° C. 2-Thiophenesulfonyl chloride (287 mg, 1.57 mmol) dissolved in dichloromethane (2.5 ml) was carefully added to the reaction mixture. The resulting mixture was stirred at −78° C. for 1 h, and at room temperature overnight. Water was added to the reaction, the phases were separated and the organic phase washed with water and dried. The solvent was removed under reduced pressure and separation by preparatory HPLC gave the title compound (110 mg, 83%) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07799804B2
Source datasetuspto-grants-2010_09
ORD IDord-5af73e5697ec4632aa77d6815530d162
Source noteuspto-grants-2010_09