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HRID 5740作成日:2026年10月23日

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

https://huagongshe.com/ja/reaction/5740

反応式

関与物質

役割名称HCID仕込み量
反応物N-(2-Aminoethyl)isoquinoline-5-sulfonamideHCID 3544—
反応物Ethyl AcetateHCID 8857—
反応物p-ChlorocinnamaldehydeHCID 3794977—
反応物SodiumHCID 5360545—
溶媒MethanolHCID 887—
生成物N-[2-(4-Chlorocinnamylamino)ethyl]-5-isoquinolinesulfonamideHCID 17615671.5%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05245034
出典データセットuspto-grants-1993_09
ORD IDord-972b7e9615b641608f2fd7c85b62dfc9
出典メモuspto-grants-1993_09