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HRID 40537생성일: 2026년 10월 23일

Triethylamine → 5-Phenylethynyl-pyridin-2-ylamine

https://huagongshe.com/ko/reaction/40537

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물PhenylacetyleneHCID 10821—
반응물2-Pyridinamine, 5-iodo-HCID 88579—
촉매TriphenylphosphineHCID 11776—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
촉매Dichlorobis(triphenylphosphine)palladiumHCID 6102075—
용매TetrahydrofuranHCID 8028—
생성물5-Phenylethynyl-pyridin-2-ylamineHCID 4685419062%

반응 조건

온도65 °C

반응 단계

Bis-(triphenylphosphine)-palladium(II)dichloride (480 mg, 0.68 mmol, 0.05 equiv.) was dissolved in 50 ml THF. (3 g, 13.6 mmol) 2-Amino-5-iodopyridine and phenylacetylene (2.79 g, 27.3 mmol, 2.0 equiv.) were added at room temperature. Triethylamine (5.58 ml, 40.9 mmol, 3 equiv.), triphenylphosphine (111 mg, 0.41 mmol, 0.03 equiv.) and copper(I)iodide (70 mg, 0.41 mmol, 0.03 equiv.) were added and the mixture was stirred for 2 hours at 65° C. The reaction mixture was cooled and extracted with saturated NaHCO3 solution and three times with ethyl acetate. The organic layers were combined, dried over sodium sulfate and evaporated to dryness. The crude product was suspended in dichloromethane, filtered and the solid evaporated to dryness. The desired 5-phenylethynyl-pyridin-2-ylamine (1.6 g, 62% yield) was obtained as a light yellow solid, MS: m/e=195.3 (M+H+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08530472B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-9ef69a63f7664327a076ce403c75816c
출처 메모uspto-grants-2013_09