戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 12858作成日:2026年10月27日

2-Aminoadamantane hydrochloride → 1-tert-butyl-5-chloro-1H-pyrazole-4-carboxylic acid adamantan-2-ylamide

https://huagongshe.com/reaction/12858

反応式

関与物質

役割名称HCID仕込み量
反応物2-Aminoadamantane hydrochlorideHCID 25331—
反応物DiisopropylethylamineHCID 81531—
反応物2-(2,5-Dioxopyrrolidin-1-yl)-1,1,3,3-tetramethylisouronium tetrafluoroborateHCID 9857522—
反応物1-(tert-Butyl)-5-chloro-1H-pyrazole-4-carboxylic acidHCID 53423553—
溶媒dichloromethane N,N-dimethylformamideHCID 22350042—
生成物1-tert-butyl-5-chloro-1H-pyrazole-4-carboxylic acid adamantan-2-ylamideHCID 2501441780%

反応手順

To a stirred solution of 1-tert-butyl-5-chloro-1H-pyrazole-4-carboxylic acid (3.040 g; 15.0 mmol) in N,N-dimethylformamide/methylene chloride (1:4 ratio, 20 mL) at room temperature was added diisopropylethylamine (21.2 mL; 120.4 mmol). TSTU (5.420 g; 18.0 mmol) was then added. The resulting mixture was allowed to stir at room temp. for 2 hr and then 2-adamantylamine hydrochloride (2.844 g; 15.0 mmol) was added. The mixture was allowed to stir over the weekend at room temperature and then concentrated in vacuo. The residue was partitioned between ethyl acetate and water. The organic layer was washed with brine, dried over sodium sulfate, filtered and concentrated in vacuo. The resulting light yellow gum was triturated with diethyl ether to provide 1-tert-butyl-5-chloro-1H-pyrazole-4-carboxylic acid adamantan-2-ylamide (4.02 g, 80%) as a white powder.

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-32b0a4940c424d8aa6d1a6599c794229
出典メモuspto-grants-2010_06