돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 12858생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/12858

반응식

참여 물질

역할이름HCID투입량
반응물2-Aminoadamantane hydrochlorideHCID 25331—
반응물DiisopropylethylamineHCID 81531—
반응물2-(2,5-Dioxopyrrolidin-1-yl)-1,1,3,3-tetramethylisouronium tetrafluoroborateHCID 9857522—
반응물1-(tert-Butyl)-5-chloro-1H-pyrazole-4-carboxylic acidHCID 53423553—
용매dichloromethane N,N-dimethylformamideHCID 22350042—
생성물1-tert-butyl-5-chloro-1H-pyrazole-4-carboxylic acid adamantan-2-ylamideHCID 2501441780%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728029B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-32b0a4940c424d8aa6d1a6599c794229
출처 메모uspto-grants-2010_06