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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482022Generated: October 27, 2026

Sodium Hydroxide → (2-(5-Chloro-2-methoxybenzoylamino)ethyl]-5-(methylaminocarbonylaminosulfonyl)thiophene

https://huagongshe.com/reaction/482022

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant2,2,2-Trichloro-n-methylacetamideHCID 248652—
Reactant2-[2-(5-Chloro-2-methoxybenzoylamino)ethyl]-5-sulfamoylthiopheneHCID 15288672—
SolventDimethyl SulfoxideHCID 679—
Product(2-(5-Chloro-2-methoxybenzoylamino)ethyl]-5-(methylaminocarbonylaminosulfonyl)thiopheneHCID 9802837—

Reaction Conditions

Temperature65 °C

Reaction Steps

120 mg of powdered NaOH and 141 mg of N-methyltrichloro-acetamide (0.8 mmol) were added to 299 mg (0.8 mmol) of 2-[2-(5-chloro-2-methoxybenzoylamino)ethyl]-5-sulfamoyl-thiophene in 9 ml of DMSO. The mixture was stir 65° C. for 1.5 hours. After cooling, it was stirred into ice water of pH 2. The precipitate was filtered off with suction and taken up in CH2Cl2, and the solution was washed with water and dried using MgSO4. After evaporating the solvent, a yellow-brown crude product remained which, after treatment with CH2Cl2 /5% methanol, crystallized at -4° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05792788
Source datasetuspto-grants-1998_08
ORD IDord-16b3842ff8724a55bc81d390fd245322
Source noteuspto-grants-1998_08