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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1248761Generated: October 25, 2026

Chloroform → N-[2-(N-methyl-N-benzylamino)ethyl]-5-isoquinolinesulfonamide

https://huagongshe.com/reaction/1248761

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantTriethylamineHCID 8471—
Reactant(2-Aminoethyl)(benzyl)methylamineHCID 3014812—
Reactant5-Isoquinolinesulfonyl chlorideHCID 3371655—
SolventDichloromethaneHCID 6344—
ProductN-[2-(N-methyl-N-benzylamino)ethyl]-5-isoquinolinesulfonamideHCID 2025429584%

Reaction Steps

In 70 ml of methylene chloride were dissolved 3.24 g of 2-(N-methyl-N-benzylamino)ethylamine and 2.0 g of triethylamine, and to the solution was added dropwise 50 ml of a methylene chloride solution containing 3.0 g of 5-isoquinolinesulfonyl chloride under cooling with ice. After the dropwise addition of the methylene chloride solution, the mixed solution was stirred at a temperature of 15° C. to 25° C. for one hour, and then the reaction solution was washed with water and extracted with a 10% aqueous hydrochloric acid solution. The aqueous layer was washed with chloroform, rendered alkaline with a 1N aqueous sodium hydroxide solution, extracted with chloroform, and then the chloroform layer was washed with water, dried with anhydrous magnesium sulfate and the chloroform was distilled therefrom under reduced pressure. The residue thus obtained was subjected to a silica gel column chromatography (silica gel: 100 g; solvent: chloroform) to give 3.84 g of N-[2-(N-methyl-N-benzylamino)ethyl]-5-isoquinolinesulfonamide, i.e., Compound (65) in a yield of 84%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04525589
Source datasetuspto-grants-1985_06
ORD IDord-5caaab0dca6b4a2ba1a3e0ddcac4bc2e
Source noteuspto-grants-1985_06