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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1889619Generated: October 27, 2026

Triethylamine → N-(Biphenyl-4-ylmethyl)-3,5-dichloro-N-(3-((4-cyanophenylsulfonamido)methyl)benzyl)-2-hydroxybenzenesulfonamide

https://huagongshe.com/reaction/1889619

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Cyanobenzenesulfonyl chlorideHCID 39497—
ReactantN-(3-(Aminomethyl)benzyl)-N-(biphenyl-4-ylmethyl)-3,5-dichloro-2-hydroxybenzenesulfonamideHCID 58531388—
SolventDichloromethaneHCID 6344—
ProductN-(Biphenyl-4-ylmethyl)-3,5-dichloro-N-(3-((4-cyanophenylsulfonamido)methyl)benzyl)-2-hydroxybenzenesulfonamideHCID 6663408660.2%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of 4-cyanobenzene-1-sulfonyl chloride (26 mg, 0.13 mmol) in CH2Cl2 (3 ml) was added Et3N (0.07 ml, 0.49 mmol) followed by N-(3-(aminomethyl)benzyl)-N-(biphenyl-4-ylmethyl)-3,5-dichloro-2-hydroxybenzenesulfonamide (65 mg, 0.12 mmol) at rt under nitrogen. The reaction mixture was stirred at 25° C. for 2 h. It was concentrated and the residue was purified by preparative HPLC. Fractions containing the desired product were combined, concentrated, and lyophilized to give the product as a white solid (50 mg, 56%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501992B2
Source datasetuspto-grants-2013_08
ORD IDord-e038c49ad2014672ae85f97496557b92
Source noteuspto-grants-2013_08