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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 365408Generated: October 31, 2026

4-[(4-Methylbenzene-1-sulfonyl)amino]benzoyl chloride → (+/-)-cis-N-[2-(3,4-dimethoxyphenyl)cyclohexyl]-4-p-toluenesulfonamidobenzamide

https://huagongshe.com/reaction/365408

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-[(4-Methylbenzene-1-sulfonyl)amino]benzoyl chlorideHCID 308905—
Reactant(-)-cis-1,2-Dimethoxy-4-(2-aminocyclohexyl)benzeneHCID 14321190—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
Product(+/-)-cis-N-[2-(3,4-dimethoxyphenyl)cyclohexyl]-4-p-toluenesulfonamidobenzamideHCID 15410434—

Reaction Steps

6.4 g of (+/-)-cis-1,2-dimethoxy-4-(2-aminocyclohexyl)benzene are dissolved in 150 ml of methylene chloride and 9 ml of triethylamine. A solution of 11.2 g of 4-p-toluenesulfonamidobenzoyl chloride in 200 ml of methylene chloride is added dropwise at RT in the course of 3 h, and the mixture is extracted after stirring for 1 h with 100 ml each of water, 2N hydrochloric acid, satd. sodium hydrogencarbonate solution and water again. The organic phase is dried using sodium sulfate, concentrated and crystallized from ethyl acetate. 3.9 g (28.2% of theory) of the title compound of m.p. 174-176° C. are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06127378
Source datasetuspto-grants-2000_10
ORD IDord-d413dfad26ca4e61afe3f7f6ec04f9b6
Source noteuspto-grants-2000_10