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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1090584Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1090584

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-(2-Aminoethyl)isoquinoline-5-sulfonamideHCID 3544—
EduktEthyl AcetateHCID 8857—
Eduktp-ChlorocinnamaldehydeHCID 3794977—
EduktSodiumHCID 5360545—
LösungsmittelMethanolHCID 887—
ProduktN-[2-(4-Chlorocinnamylamino)ethyl]-5-isoquinolinesulfonamideHCID 17615671,5%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05081246
Quelldatensatzuspto-grants-1992_01
ORD IDord-28f2fa3e29714c79baf4ba04a2944ec3
Quellennotizuspto-grants-1992_01