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HRID 464104作成日:2026年10月26日

Water → 5-Amino-4-cyano-1-(5-trimethylsilyl-4-pentynyl)pyrazole

https://huagongshe.com/reaction/464104

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Potassium CarbonateHCID 11430—
反応物5-Amino-4-cyanopyrazoleHCID 85515—
反応物Silane, (5-iodo-1-pentynyl)trimethyl-HCID 11140046—
溶媒ChloroformHCID 6212—
溶媒DimethylformamideHCID 6228—
生成物5-Amino-4-cyano-1-(5-trimethylsilyl-4-pentynyl)pyrazoleHCID 2026383320.4%

反応手順

A suspension of 5-amino-4-cyanopyrazole (10 g) and finely ground anhydrous potassium carbonate (38 g) in dry DMF (100 ml) was treated with 5-iodo-1-trimethylsilyl-1-pentyne (25 g) and the mixture was stirred under nitrogen for two days at room temperature. The reaction mixture was then poured into water and the product extracted into ethyl acetate. The extract was washed with water and then with brine, dried over Na2SO4, and evaporated to give a semisolid brown residue. This solid was taken up in chloroform and filtered through a short plug of silica gel. Evaporation of the chloroform left a tan solid comprising a mixture of the isomeric compounds 5-amino-4-cyano-1-(5-trimethylsilyl-4-pentynyl)pyrazole and 3-amino-4-cyano-1-(5-trimethylsilyl-4-pentynyl)pyrazole. Fractional recrystallization from ethyl acetate/hexane gave 4.66 grams of the desired 5-amino-4-cyano-1-(5-trimethylsilyl-4-pentynyl)pyrazole: mp 125°-127°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04546104
出典データセットuspto-grants-1985_10
ORD IDord-0bebbb73c7e44a5eadcc029bcc5de8fb
出典メモuspto-grants-1985_10