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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1984640생성일: 2026년 10월 26일

Triethylamine → 2-(5-Methyl-3-phenyl-isoxazol-4-ylethynyl)-pyridine

https://huagongshe.com/reaction/1984640

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물1,3-Bis(diphenylphosphino)propaneHCID 81219—
반응물EthynylpyridineHCID 137268—
반응물4-Iodo-5-methyl-3-phenylisoxazoleHCID 2776150—
촉매palladium(II) acetateHCID 167845—
용매DimethylformamideHCID 6228—
생성물2-(5-Methyl-3-phenyl-isoxazol-4-ylethynyl)-pyridineHCID 2478444623.1%

반응 조건

온도90 °C

반응 단계

A mixture of 4-iodo-5-methyl-3-phenylisoxazole (285 mg, 1.00 mmol), palladium(II) acetate (7 mg, 0.03 mmol), 1,3-bis(diphenylphosphino)propane (12 mg, 0.03 mmol), triethylamine (348 μL, 2.50 mmol) and 2-ethynylpyridine (131 μL, 1.30 mmol) in N,N-dimethylformamide (2 mL) was evaporated and flushed with argon. Cuprous iodide (4 mg, 0.02 mmol) was added and the reaction mixture was stirred for 3 h at 90° C. before cooling to ambient temperature and separated between aqueous sodium hydroxide (1 M, 30 mL) and ethyl acetate (50 mL). The aqueous layer was extracted with ethyl acetate (50 mL) and washed with aqueous sodium hydroxide (1 M, 30 mL). The combined organic layers were dried over sodium sulfate and concentrated. Purification by chromatography (SiO2, heptane:ethyl acetate=100:0 to 67:33) afforded the title compound (60 mg, 23%) as a light brown solid. MS: m/e=261.2 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07544704B2
출처 데이터셋uspto-grants-2009_06
ORD IDord-cfb5c6edebff49b29fea7c3ae5467541
출처 메모uspto-grants-2009_06