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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 8217생성일: 2026년 10월 23일

Triethylamine → 4-Pyridin-2-ylethynyl-quinoline-2-carboxylic Acid Ethyl Ester

https://huagongshe.com/ko/reaction/8217

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물EthynylpyridineHCID 137268—
반응물Ethyl 4-bromoquinoline-2-carboxylateHCID 21992780—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
촉매Dichlorobis(triphenylphosphine)palladiumHCID 6102075—
용매AcetonitrileHCID 6342—
생성물4-Pyridin-2-ylethynyl-quinoline-2-carboxylic Acid Ethyl EsterHCID 6936490150.3%

반응 조건

온도77.5 °C

반응 단계

A mixture of ethyl 4-bromoquinoline-2-carboxylate (2.80 g, 10.0 mmol, J. Org. Chem. 1947, 12, 456), triethylamine (1.7 mL, 12 mmol), bis(triphenylphosphine)-palladium(II)chloride (0.561 g, 0.80 mmol), CuI (0.114 g, 0.60 mmol), and 2-ethynylpyridine (1.11 g, 10.8 mmol) in CH3CN (80 mL) is heated at 75-80° C. for 18 h in a sealed tube. Additional triethylamine (0.85 ml, 6.1 mmol), bis(triphenylphosphine)palladium (II) chloride (0.23 g, 0.40 mmol), and CuI (0.055 g, 0.29 mmol) is added and the mixture heated for an additional 18 h. The mixture is concentrated in vacuo and partitioned between water and chloroform. The chloroform extracts are washed with brine and evaporated. The residue is chromatographed on SiO2 (50% ethyl acetate/hexanes) to yield 1.52 g (50%) of a yellow solid. Precipitation from ethyl acetate gave the title compound as yellow crystals: mp 129-131° C.; MS ES+ m/e 303 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087626B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-9dbb6f48418e4ea8ad11976c7e04ceca
출처 메모uspto-grants-2006_08