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HRID 1633917作成日:2026年10月27日

P-Toluenesulfonylhydrazide → 4-[(4-Cyclopropylcyclohexylamino)methyl]benzoic acid methyl ester

https://huagongshe.com/reaction/1633917

反応式

関与物質

役割名称HCID仕込み量
反応物P-ToluenesulfonylhydrazideHCID 15303—
反応物4-[(4-Cyclopropylidenecyclohexylamino)methyl]benzoic acid methyl esterHCID 23550140—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物4-[(4-Cyclopropylcyclohexylamino)methyl]benzoic acid methyl esterHCID 23550139—

反応条件

温度100 °C

反応手順

4-[(4-Cyclopropylidenecyclohexylamino)methyl]benzoic acid methyl ester (1.1 g, 3.9 mmol) was dissolved in DMF (40 mL) and p-toluenesulfonic acid hydrazide (2.8 g, 15.4 mmol) was added. The reaction was heated to 100° C. for 16 hours. After cooling to room temperature the reaction mixture was diluted with ethyl acetate (75 mL) and water (40 mL) was added. The aqueous phase was extracted with ethyl acetate (25 mL) and the combined organic phases washed with aqueous saturated sodium hydrogen carbonate (2×30 mL) and water (5×30 mL). The organic phase was dried (MgSO4) and concentrated in vacuo. The residue was purified by flash chromatography (25 g silica) using heptane and ethyl acetate (1:1) as eluent to give 4-[(4-cyclopropylcyclohexylamino)methyl]benzoic acid methyl ester.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06503949B1
出典データセットuspto-grants-2003_01
ORD IDord-3d46ad9a739e4d60a06b417c1322a365
出典メモuspto-grants-2003_01