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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 20755생성일: 2026년 10월 25일

Trimethylsilylacetylene → 2-(4-ethynyl-2-fluoroanilino)-3,4-difluoro-N-(2-hydroxyethoxy)-5-[(E)-(2-hydroxy-2-methylpropoxy)iminomethyl]benzamide

https://huagongshe.com/reaction/20755

반응식

참여 물질

역할이름HCID투입량
반응물TrimethylsilylacetyleneHCID 66111—
반응물DiisopropylethylamineHCID 81531—
반응물Tetrabutylammonium FluorideHCID 2724141—
반응물Trisodium 3,3',3''-phosphinetriyltris(benzene-1-sulphonate)HCID 6099338—
반응물3,4-difluoro-2-(2-fluoro-4-iodoanilino)-N-(2-hydroxyethoxy)-5-[(E)-(2-hydroxy-2-methylpropoxy)iminomethyl]benzamideHCID 11387506—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매MethanolHCID 887—
용매Ethyl AcetateHCID 8857—
생성물2-(4-ethynyl-2-fluoroanilino)-3,4-difluoro-N-(2-hydroxyethoxy)-5-[(E)-(2-hydroxy-2-methylpropoxy)iminomethyl]benzamideHCID 11363286574.9%

반응 단계

(E)-3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-hydroxy-2-methyl-propoxyimino)-methyl]-benzamide (200 mg, 0.35 mmol), Pd(CH3CN)2Cl2 (4.5 mg, 0.0176 mmol), triphenylphosphine-3,3′,3″-trisulfonic acid trisodium salt (25.0 mg, 0.037 mmol), N(iPr)2Et (48.0 mg, 0.37 mmol), trimethylsilyl acetylene (172 mg, 1.76 mmol), and CuI (3.4 mg, 0.0176 mmol) were stirred in MeOH at room temperature for 1 hour, and the solvent was evaporated. The resultant residue was added to THF/H2O containing tetrabutylammonium fluoride (0.35 mmol), and the mixture was stirred for 1 hour. EtOAc was added thereto, and the organic layer was washed with 0.4 N aqueous HCl, dried over Na2SO4, and evaporated. The resultant residue was purified by silica gel chromatography (CH2Cl2/MeOH as a developing solvent) to give a title compound (99 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745663B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-b156245e9c11473f9faf23341a2f78ad
출처 메모uspto-grants-2010_06