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HRID 238668作成日:2026年10月25日

Potassium Hydroxide → 1-[2-[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]acetyl]-4-piperidinecarbonitrile

https://huagongshe.com/reaction/238668

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium HydroxideHCID 14797—
反応物1H-Pyrazole, 3-methyl-5-(trifluoromethyl)-HCID 139077—
反応物1-(2-Chloroacetyl)piperidine-4-carbonitrileHCID 67470097—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物1-[2-[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]acetyl]-4-piperidinecarbonitrileHCID 67470637—

反応条件

温度7.5 °C

反応手順

A solution of 3-methyl-5-trifluoromethylpyrazole (9.3 g, 62 mmol) and 45% aqueous potassium hydroxide solution (7.79 g, 62 mmol) in N,N-dimethylformamide (25 mL) was cooled to 5° C., and 1-(2-chloroacetyl)-4-piperidinecarbonitrile (i.e. the product of Example 8, Step A or A1) (11.2 g, 60 mmol) was added. The reaction mixture was stirred for 8 h at 5-10° C., then diluted with water (100 mL), and filtered. The filter cake was washed with water and dried at 50° C. in a vacuum-oven to give 15 g of the title compound as a solid containing 3% of its regioisomer, i.e. 1-[2-[3-methyl-5-(trifluoromethyl)-1H-pyrazol-1-yl]acetyl]-4-piperidinecarbonitrile.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08642634B2
出典データセットuspto-grants-2014_02
ORD IDord-3cb205934601414d8db1b645cc1d22b7
出典メモuspto-grants-2014_02