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HRID 12853作成日:2026年10月24日

Pyrazole → 2'-tert-butyl-2'H-[1,3']bipyrazolyl-4'-carboxylic acid adamantan-2-ylamide

https://huagongshe.com/ja/reaction/12853

反応式

関与物質

役割名称HCID仕込み量
反応物PyrazoleHCID 1048—
反応物Potassium FluorideHCID 522689—
反応物1-tert-butyl-5-chloro-1H-pyrazole-4-carboxylic acid adamantan-2-ylamideHCID 25014417—
溶媒Dimethyl SulfoxideHCID 679—
生成物2'-tert-butyl-2'H-[1,3']bipyrazolyl-4'-carboxylic acid adamantan-2-ylamideHCID 1674254041%

反応手順

In a Personal Chemistry microwave process tube (Biotage AB, Sweden), 1-tert-butyl-5-chloro-1H-pyrazole-4-carboxylic acid adamantan-2-ylamide (Example 36, 100 mg, 0.30 mmol), pyrazole (41 mg, 0.60 mmol), KF (35 mg, 0.60 mmol) and DMSO (2 mL) were well mixed. The tube was sealed with a septum and was submitted to 150 W microwave irradiation using a Personal Chemistry Microwave Synthesis system (Biotage AB, Sweden) at 230° C. for 20 minutes. The reaction mixture was partitioned between ethyl acetate and water and the aqueous phase was extracted three times with ethyl acetate. The organic phases were combined, concentrated in vacuo and purified by C-18 reversed phase prep-HPLC with a gradient of 10-100% acetonitrile/water to give 2′-tert-butyl-2′H-[1,3′]bipyrazolyl-4′-carboxylic acid adamantan-2-ylamide (45 mg, 41%). Mass spectrum: m/z: 368.2 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07728029B2
出典データセットuspto-grants-2010_06
ORD IDord-c38d0564c8994c85877cb4441405fdcf
出典メモuspto-grants-2010_06