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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 339125생성일: 2026년 10월 26일

Hydrochloric Acid → 2-Chloro-N-cyclopropyl-4-[3-oxo-3-({2,2,2-trifluoro-1-[3-(trifluoromethyl)phenyl]ethyl}amino)-prop-1-yn-1-yl]benzamide

https://huagongshe.com/reaction/339125

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물DiisopropylamineHCID 7912—
반응물Propiolic AcidHCID 10110—
반응물4-(4,6-Dimethoxy[1.3.5]triazin-2-yl)-4-methylmorpholinium chloride hydrateHCID 23149411—
반응물2,2,2-Trifluoro-1-(3-(trifluoromethyl)phenyl)ethanamineHCID 43825172—
반응물2-chloro-N-cyclopropyl-4-iodobenzamideHCID 58247943—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
촉매HCID 178418476HCID 178418476—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물2-Chloro-N-cyclopropyl-4-[3-oxo-3-({2,2,2-trifluoro-1-[3-(trifluoromethyl)phenyl]ethyl}amino)-prop-1-yn-1-yl]benzamideHCID 58247932—

반응 조건

온도0 °C

반응 단계

2-Chloro-N-cyclopropyl-4-iodobenzamide (1.0 g, 3.11 mmol) and propiolic acid (222 mg, 3.11 mmol) were dissolved in N,N-dimethylformamide (1.2 ml) and cooled to 0° C. Then bis(triphenylphosphine)palladium(II) dichloride (43 mg, 0.06 mmol) and copper(I) iodide (23 mg, 0.12 mmol) were added and the mixture was cooled to −10° C. After addition of diisopropylamine (786 mg, 7.77 mmol), the mixture was warmed slowly to room temperature and stirred overnight. The reaction mixture was diluted with ethyl acetate, washed successively with hydrochloric acid (2 M) and saturated sodium chloride solution, dried over magnesium sulphate, filtered and concentrated to dryness under reduced pressure. The residue was dissolved in N,N-dimethylformamide (1 ml) and admixed with 4-(4,6-dimethoxy[1.3.5]triazin-2-yl)-4-methylmorpholinium chloride hydrate (973 mg, 3.52 mmol) and 2,2,2-trifluoro-1-[3-trifluoromethylphenyl]ethanamine (780 mg, 3.20 mmol) and stirred at room temperature overnight. The reaction solution was admixed with hydrochloric acid (1 M) and extracted with ethyl acetate. The organic phase was washed with saturated sodium hydrogencarbonate solution and saturated sodium chloride solution, dried over sodium sulphate, filtered and concentrated to dryness under reduced pressure. The residue was purified by means of silica gel chromatography with the eluent cyclohexane/ethyl acetate (EA) (0% EA to 40% EA).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08889878B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-0e70a4397434488785954eefe2989417
출처 메모uspto-grants-2014_11