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HRID 861435생성일: 2026년 10월 26일

Triethylamine → 3-[2-(4-[1,3,4-Oxadiazol-2-yl]phenyl)ethynyl]-3-hydroxyquinuclidine

https://huagongshe.com/reaction/861435

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물2-(4-Bromophenyl)-1,3,4-oxadiazoleHCID 715120—
반응물3-Ethynyl-1-azabicyclo[2.2.2]octan-3-olHCID 3613517—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
촉매Dichlorobis(triphenylphosphine)palladiumHCID 6102075—
용매DimethylformamideHCID 6228—
생성물3-[2-(4-[1,3,4-Oxadiazol-2-yl]phenyl)ethynyl]-3-hydroxyquinuclidineHCID 1970313839.2%

반응 조건

온도65 °C

반응 단계

A mixture of 3-ethynyl-3-hydroxyquinuclidine (1.06 g), 2-(4-bromopbenyl)-1,3,4-oxadiazole (1.58 g), bis(triphenylphosphine)palladium (II) chloride (245 mg), copper (I) iodide (123 mg), triethylamine (7 ml) and dimethylformamide (14 ml) were heated at 65° C. under an atmosphere of argon for 4 hours. The triethylamine and DHF were removed by evaporation. An aqueous solution of sodium hydroxide (2M, 20 ml) was added to the residue and the mixture extracted with dichloromethane (3×30 ml). The organic extracts were combined, dried (MgSO4) and evaporated. The residue was purified by flash column chromatography on silica gel eluting with 10% methanol in dichloromethane containing 1% ammonia (density 0.88 g/cm3) to give 3-[2-(4-[1,3,4-oxadiazol-2-yl]phenyl)ethynyl]-3-hydroxyquinuclidine (811 mg) as a solid, m.p. 229-230%; microanalysis, found: C, 67.9; H, 5.8; N, 14.2%; C17H17N3O3. 0.4 H2O requires: C, 67.5; H, 5.9; N, 13.9; NMR: 1.20-1.44(1H,m), 1.50-1.71(1H,m), 1.77-2.04(3H,m), 2.69(4H,t), 2.79-2.94(1H,d), 3.04-3.20(1H,d), 5.69(1H,s), 7.63(2H,d), 8.03(2H,d), 9.35(1H,s); m/z 296(M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05714496
출처 데이터셋uspto-grants-1998_02
ORD IDord-47dafcefd273432498f1a76304ffae4d
출처 메모uspto-grants-1998_02