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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | 2-Pyrimidinamine, 5-chloro- | HCID 79479 | — |
| 반응물 | 4-(3-(3,5-Dichlorophenyl)-4,4,4-trifluoro-2-butenoyl)benzoic acid chloride | HCID 87129944 | — |
| 용매 | Pyridine | HCID 1049 | — |
| 생성물 | N-(5-chloro-2-pyrimidinyl)-4-(3-(3,5-dichlorophenyl)-4,4,4-trifluoro-2-butenoyl)benzoic acid amide | HCID 86626430 | 50.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07700808B2 |
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| 출처 데이터셋 | uspto-grants-2010_04 |
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| ORD ID | ord-936156af533845649de82c1a29311ee4 |
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| 출처 메모 | uspto-grants-2010_04 |
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