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HRID 1280544作成日:2026年10月25日

3-Methyl-2-thiophenecarboxaldehyde → (3-Methylthien-2-ylmethyl)-[4-(5-methylthio-3-pyridin-4-yl-1H-1,2,4-triazol-1-yl)phenyl]amine

https://huagongshe.com/reaction/1280544

反応式

関与物質

役割名称HCID仕込み量
反応物3-Methyl-2-thiophenecarboxaldehydeHCID 79911—
反応物Sodium cyanoborohydrideHCID 5003444—
反応物1-(4-aminophenyl)-5-methylthio-3-(4-pyridyl)-1H-1,2,4-triazoleHCID 18425871—
溶媒Acetic AcidHCID 176—
溶媒MethanolHCID 887—
生成物(3-Methylthien-2-ylmethyl)-[4-(5-methylthio-3-pyridin-4-yl-1H-1,2,4-triazol-1-yl)phenyl]amineHCID 18425879—

反応手順

A stirred solution of 1-(4-aminophenyl)-5-methylthio-3-(4-pyridyl)-1H-1,2,4-triazole (Example 1) (100 mg, 0.35 mmol) and 3-methylthiophene-2-carboxaldehyde (44 mg, 0.35 mmol) in 5% acetic acid in MeOH (4 mL) at room temperature was treated with sodium cyanoborohydride (55 mg, 0.88 mmol) and the reaction mixture was further stirred at room temperature for 48 h. The reaction mixture was concentrated, diluted with EtOAc, washed with NaHCO3 solution, brine and dried (MgSO4). The residue obtained on concentration was flash chromatographed on silica gel and eluted with a gradient of dichloromethane/acetone (9/1 to 3/1). The title compound was obtained as a white solid (85 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06451820B1
出典データセットuspto-grants-2002_09
ORD IDord-34d645a9fa704ad29676d2a9f47237ce
出典メモuspto-grants-2002_09