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HRID 5743作成日:2026年10月25日

Formic Acid → N-[2-(N-formyl-p-chlorocinnamylamino)ethyl]-5-isoquinolinesulfonamide

https://huagongshe.com/reaction/5743

反応式

関与物質

役割名称HCID仕込み量
反応物Formic AcidHCID 284—
反応物Acetic AnhydrideHCID 7918—
反応物Sodium CarbonateHCID 10340—
反応物N-[2-(4-Chlorocinnamylamino)ethyl]-5-isoquinolinesulfonamideHCID 176156—
溶媒Ethyl AcetateHCID 8857—
生成物N-[2-(N-formyl-p-chlorocinnamylamino)ethyl]-5-isoquinolinesulfonamideHCID 131319—

反応手順

3 ml of formic acid and 3 ml of acetic anhydride were mixed and stirred at a room temperature, and to the mixture was added 1.41 g of the product of Example 172, and the mixture was stirred for one hour. The reaction mixture was added to 50 ml of ethyl acetate and 30 ml of saturated sodium carbonate aqueous solution with ice, and the mixture was stirred, and after foaming was terminated, the ethyl acetate layer was sequentially washed twice with water and once with a saturated sodium chloride aqueous solution, and dried over magnesium sulfate, filtered and evaporated under a reduced pressure. The resulting residue was purified on a silica gel column (silica gel 60 g, eluant: 2% methanol in chloroform), to obtain 1.49 g of the title compound as a mixture of two isomers (3:2) in a colorless amorphous form.

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-bdd40074d9ed4c75ae6e98ec6d069c3c
出典メモuspto-grants-1993_09