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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1090584Generated: October 27, 2026

N-(2-Aminoethyl)isoquinoline-5-sulfonamide → N-[2-(4-Chlorocinnamylamino)ethyl]-5-isoquinolinesulfonamide

https://huagongshe.com/reaction/1090584

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(2-Aminoethyl)isoquinoline-5-sulfonamideHCID 3544—
ReactantEthyl AcetateHCID 8857—
Reactantp-ChlorocinnamaldehydeHCID 3794977—
ReactantSodiumHCID 5360545—
SolventMethanolHCID 887—
ProductN-[2-(4-Chlorocinnamylamino)ethyl]-5-isoquinolinesulfonamideHCID 17615671.5%

Reaction Steps

2.01 g of N-(2-aminoethyl)-5-isoquinolinesulfonamide was dissolved in 30 ml of methanol, to the solution was added 1.60 g of p-chlorocinnamaldehyde, and the mixture was stirred for one hour at a room temperature. After an addition of 350 mg of sodium tetrahydrideborate in portions with ice cooling, the mixture was stirred for 30 minutes. After an addition of ethyl acetate, the reaction mixture was sequentially washed three times with water, and then twice with a saturated sodium chloride aqueous solution, and dried over magnesium sulfate. The mixture was filtered and evaporated to remove the solvent under a reduced pressure. A residue was purified using a silica gel column (silica gel 80 g, eluant: 5% methanol in chloroform), and resulting crystals were washed with benzene/hexane (1:1), to obtain 2.30 g of the title compound as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05081246
Source datasetuspto-grants-1992_01
ORD IDord-28f2fa3e29714c79baf4ba04a2944ec3
Source noteuspto-grants-1992_01