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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 602005생성일: 2026년 10월 23일

Ammonium Chloride → N-(2-chlorocyclohexyl)-3,5-difluoro-4-(2-propynyloxy)benzamide

https://huagongshe.com/ko/reaction/602005

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물7-[3,5-Difluoro-4-(2-propynyloxy)benzoyl]-7-azabicyclo[4.1.0]heptaneHCID 57701178—
촉매ZincchlorideHCID 3007855—
용매ChloroformHCID 6212—
생성물N-(2-chlorocyclohexyl)-3,5-difluoro-4-(2-propynyloxy)benzamideHCID 57701136—

반응 조건

온도60 °C

반응 단계

A mixture of 4 ml of chloroform and 298 mg of zinc (II) chloride was stirred at 60° C. After 5 minutes, a mixture of 291 mg of 7-[3,5-difluoro-4-(2-propynyloxy)benzoyl]-7-azabicyclo[4.1.0]heptane and 2 ml of chloroform was added dropwise thereto at 60° C., and the resulting mixture was heated under reflux for 5 hours. Then, an aqueous saturated ammonium chloride solution was added to the reaction mixture, and this was extracted with chloroform. The organic layer was dried over magnesium sulfate, and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to obtain 0.22 g of N-(2-chlorocyclohexyl)-3,5-difluoro-4-(2-propynyloxy)benzamide (hereinafter, described as the compound 87 of the present invention) represented by the formula:

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07902400B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-9c87c08183054d25addd37cb2ab63ce0
출처 메모uspto-grants-2011_03