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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 886720생성일: 2026년 10월 26일

2,6-Dichlorobenzoyl chloride → 5-Amino-N-[2-({[(2,6-dichlorophenyl)carbonyl]amino}methyl)-3,3,3-trifluoro-2-hydroxypropyl]-1-(4-fluorophenyl)-1H-pyrazole-4-carboxamide

https://huagongshe.com/reaction/886720

반응식

참여 물질

역할이름HCID투입량
반응물2,6-Dichlorobenzoyl chlorideHCID 78392—
반응물DiisopropylethylamineHCID 81531—
반응물5-amino-N-[2-(aminomethyl)-3,3,3-trifluoro-2-hydroxypropyl]-1-(4-fluorophenyl)-1H-pyrazole-4-carboxamideHCID 59487494—
용매TetrahydrofuranHCID 8028—
생성물5-Amino-N-[2-({[(2,6-dichlorophenyl)carbonyl]amino}methyl)-3,3,3-trifluoro-2-hydroxypropyl]-1-(4-fluorophenyl)-1H-pyrazole-4-carboxamideHCID 23649465—

반응 조건

온도21 °C

반응 단계

To a solution of 5-amino-N-[2-(aminomethyl)-3,3,3-trifluoro-2-hydroxypropyl]-1-(4-fluorophenyl)-1H-pyrazole-4-carboxamide (0.93 g, 2.57 mmol) in anhydrous tetrahydrofuran (12 ml) was added diisopropylethylamine (0.91 ml, 5.2 mmol) followed by 2,6-dichlorobenzoyl chloride (0.38 ml, 1.05 equiv). There was an immediate exotherm and therefore the mixture was placed in an ice/solid carbon dioxide bath for 20 minutes and then stirred at 21° C. for 17 hours. It was then partitioned between ethyl acetate (100 ml) and 2M hydrochloric acid (20 ml) and the organic phase was washed with water (20 ml), saturated brine (20 ml), saturated sodium bicarbonate (20 ml), water (20 ml) and saturated brine (20 ml) before being dried over magnesium sulphate and evaporated under reduced pressure to give a foam. This was purified on a Flashmaster column of silica (100 g) with a gradient of 0-100% ethyl acetate in cyclohexane over 60 minutes to give the title compound (1.07 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08247377B2
출처 데이터셋uspto-grants-2012_08
ORD IDord-638c01ecf1f74151b4d7c511c85493f5
출처 메모uspto-grants-2012_08