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HRID 1470640생성일: 2026년 10월 26일

4-Ethynyl-1,1'-biphenyl → 2-Amino-3-biphenyl-4-ylethynyl-benzoic acid methyl ester

https://huagongshe.com/reaction/1470640

반응식

참여 물질

역할이름HCID투입량
반응물4-Ethynyl-1,1'-biphenylHCID 34464—
반응물Methyl 2-amino-3-iodobenzoateHCID 21258150—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
촉매Dichlorobis(triphenylphosphine)palladiumHCID 6102075—
용매TetrahydrofuranHCID 8028—
생성물2-Amino-3-biphenyl-4-ylethynyl-benzoic acid methyl esterHCID 6670634276.4%

반응 단계

To a solution of 2-amino-3-iodo-benzoic acid methyl ester (500 mg, 1.8 mmol), 4-ethynyl-biphenyl (416 mg, 2.3 mmol) in THF (20 mL), CuI (17 mg, 0.09 mmol), bis-(triphenylphosphine)-palladium (II)-chloride (64 mg, 0.09 mmol) and TEA (0.75 mL, 5.4 mmol) were added. This mixture was stirred at room temperature for 12 h. The progress of the reaction was monitored by TLC. After completion, the reaction mass was filtered through celite, and the collected filtrate was diluted with ethyl acetate (30 mL), washed with water (2×20 mL) and the combined organic layer was separated and dried over sodium sulphate and concentrated under reduced pressure to obtain brown mass which was purified by column chromatography using 5% ethyl acetate in hexane as an eluent to obtain 450 mg of 2-amino-3-biphenyl-4-ylethynyl-benzoic acid methyl ester as a pale yellow coloured solid (76%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09006454B2
출처 데이터셋uspto-grants-2015_04
ORD IDord-ec4b4a98675e4a7e8de6f7f7588ea4e5
출처 메모uspto-grants-2015_04