돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 238368생성일: 2026년 10월 25일

4-(Trifluoromethyl)aniline → 1-methyl-N-[4-(trifluoromethyl)phenyl]-1H-pyrazole-5-carboxamide

https://huagongshe.com/reaction/238368

반응식

참여 물질

역할이름HCID투입량
반응물4-(Trifluoromethyl)anilineHCID 9964—
반응물1-methyl-1H-pyrazole-5-carboxylic acidHCID 643158—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물1-Hydroxybenzotriazole hydrateHCID 2796029—
용매ChloroformHCID 6212—
생성물1-methyl-N-[4-(trifluoromethyl)phenyl]-1H-pyrazole-5-carboxamideHCID 150991247.1%

반응 단계

A mixture of 1-methyl-1H-pyrazol-5-carboxylic acid (1.00 g), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (1.82 g), 1-hydroxybenzotriazole monohydrate (1.70 g) and chloroform (20 mL) was stirred at a room temperature for 15 minutes. Thereafter, 4-aminobenzotrifluoride (1.27 g) was added to the reaction solution, and the obtained mixture was then stirred for 24 hours. Thereafter, the reaction solution was concentrated under a reduced pressure, and the residue was then purified by column chromatography (chromatorex NH, hexane:ethyl acetate=4:1), so as to obtain the title compound (1.00 g) in the form of a colorless solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08642626B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-29142283cdf14f43877ba3074fcfb03b
출처 메모uspto-grants-2014_02