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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 14608생성일: 2026년 10월 23일

Triphenylarsine → 4-[2-(4-Pyrimidin-2-yl-phenoxy)-acetylamino]-thiophene-3-carboxylic acid methyl ester

https://huagongshe.com/ko/reaction/14608

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylarsineHCID 11773—
반응물2-(Tributylstannyl)pyrimidineHCID 2763251—
반응물4-[2-(4-Iodo-phenoxy)-acetylamino]-thiophene-3-carboxylic acid methyl esterHCID 68687330—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매DimethylformamideHCID 6228—
생성물4-[2-(4-Pyrimidin-2-yl-phenoxy)-acetylamino]-thiophene-3-carboxylic acid methyl esterHCID 6868741159.7%

반응 조건

온도90 °C

반응 단계

To 4-[2-(4-Iodo-phenoxy)-acetylamino]-thiophene-3-carboxylic acid methyl ester (77.6 mg) in DMF (1 mL) was added 2-(tributylstannyl)pyrimidine (74.1 mg), tris(dibenzylideneacetone)-di-Palladium, triphenylarsine (27 mg) and copper (I) iodide (3.2 mg) and the reaction mixture was stirred at 90° C. overnight. The reaction mixture was then allowed to cool to room temperature and was concentrated in vacuo. To the residue was then added ethylacetate (4 mL) and an aqueous solution of potassium fluoride (30%) and the mixture was stirred rigorously for one hour. Then the solid was filtered off and the biphasic filtrate was separated. The organic layer was dried with sodium sulfate and concentrated in vacuo. The residue was then purified by column chromatography to yield the title compound (41 mg, 59%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732452B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-f00d233ece4c4ef6842b8ecf31910015
출처 메모uspto-grants-2010_06