돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 645302생성일: 2026년 10월 24일

Water → N-(5-chloro-2-pyrimidinyl)-4-(3-(3,5-dichlorophenyl)-4,4,4-trifluoro-2-butenoyl)benzoic acid amide

https://huagongshe.com/ko/reaction/645302

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물2-Pyrimidinamine, 5-chloro-HCID 79479—
반응물4-(3-(3,5-Dichlorophenyl)-4,4,4-trifluoro-2-butenoyl)benzoic acid chlorideHCID 87129944—
용매PyridineHCID 1049—
생성물N-(5-chloro-2-pyrimidinyl)-4-(3-(3,5-dichlorophenyl)-4,4,4-trifluoro-2-butenoyl)benzoic acid amideHCID 8662643050.5%

반응 단계

To a solution of 0.5 g of 2-amino-5-chloropyrimidine in 20 mL of pyridine, 0.5 g of 4-(3-(3,5-dichlorophenyl)-4,4,4-trifluoro-2-butenoyl)benzoic acid chloride was poured at room temperature and the mixture was stirred for 2.5 hours. After that, water was added to the reaction solution that was extracted with ethyl acetate, an organic layer was washed with water and diluted hydrochloric acid and then dehydrated and dried with saturated saline followed by anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. The resulting residue was purified using silica gel column chromatography that was eluted with ethyl acetate-hexane (5:2) followed by crystallization from a mixed solvent of hexane and a small amount of ethyl acetate to obtain 0.31 g of aimed product as white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07700808B2
출처 데이터셋uspto-grants-2010_04
ORD IDord-936156af533845649de82c1a29311ee4
출처 메모uspto-grants-2010_04