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HRID 30718作成日:2026年10月24日

Methanesulfonic Acid → (2E)-3-[5-(4-fluorophenyl)-1-methyl-1H-pyrazol-4-yl]-N-{4-[(5-methyl-1,3,4-oxadiazol-2-yl)methyl]phenyl}acrylamide

https://huagongshe.com/ja/reaction/30718

反応式

関与物質

役割名称HCID仕込み量
反応物Methanesulfonic AcidHCID 6395—
反応物TetrahydrofuranHCID 8028—
反応物Triethyl orthoacetateHCID 66221—
反応物(2E)-3-[5-(4-fluorophenyl)-1-methyl-1H-pyrazol-4-yl]-N-[4-(2-hydrazino-2-oxoethyl)phenyl]acrylamideHCID 69209331—
溶媒Ethyl AcetateHCID 8857—
生成物(2E)-3-[5-(4-fluorophenyl)-1-methyl-1H-pyrazol-4-yl]-N-{4-[(5-methyl-1,3,4-oxadiazol-2-yl)methyl]phenyl}acrylamideHCID 6921025347.1%

反応手順

A mixture of (2E)-3-[5-(4-fluorophenyl)-1-methyl-1H-pyrazol-4-yl]-N-[4-(2-hydrazino-2-oxoethyl)phenyl]acrylamide (0.50 g), triethyl orthoacetate (0.63 g), methanesulfonic acid (0.025 g), and tetrahydrofuran (10 mL) was heated under reflux for 1 hr. The reaction mixture was diluted with ethyl acetate, washed successively with saturated aqueous sodium hydrogen carbonate and saturated brine, dried over anhydrous magnesium sulfate and concentrated. The residue was subjected to silica gel column chromatography to give (2E)-3-[5-(4-fluorophenyl)-1-methyl-1H-pyrazol-4-yl]-N-{4-[(5-methyl-1,3,4-oxadiazol-2-yl) methyl]phenyl}acrylamide as pale-yellow crystals (0.25 g, yield 46%) from a fraction eluted with ethyl acetate-methanol (100:0-20:1, v/v). Recrystallization thereof from ethyl acetate-hexane gave pale-yellow prism crystals. melting point: 151-152° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07423159B2
出典データセットuspto-grants-2008_09
ORD IDord-76a52bfb8fda4b18b22905c1ff77b86f
出典メモuspto-grants-2008_09