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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 365814생성일: 2026년 10월 27일

Water → 5-(5-Phenyl-1-pentynyl)-3-(1-methyl-2-(s)-pyrrolidinylmethoxy)pyridine

https://huagongshe.com/reaction/365814

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물5-Phenyl-1-pentyneHCID 74573—
반응물Sodium BicarbonateHCID 516892—
반응물HCID 11288721HCID 11288721—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
촉매HCID 178418476HCID 178418476—
용매DichloromethaneHCID 6344—
용매TriethylamineHCID 8471—
생성물5-(5-Phenyl-1-pentynyl)-3-(1-methyl-2-(s)-pyrrolidinylmethoxy)pyridineHCID 5425894681.9%

반응 단계

To a solution of 5-bromo-3-(1-methyl-2-(S)-pyrrolidinylmethoxy)-pyridine (408 mg, 1.50 mmol), bis(triphenylphosphine)palladium(II) chloride (21 mg, 0.029 mmol) and copper (I) iodide (5 mg, 0.029 mmol) in CH2Cl2 (3.0 mL) and NEt3 (1.0 mL) was added 5-phenyl-1-pentyne (324 mg, 2.25 mmol). The mixture was refluxed overnight then cooled to room temperature. Water (2 mL) was added, and solid sodium bicarbonate was added until the aqueous layer was saturated. The mixture was extracted with EtOAc, which was dried over MgSO4, filtered and concentrated. The residue was chromatographed on a silica gel column, eluting with NH4OH/MeOH/EtOAc 0:1:9 and 1:10:90 to afford an oil (411 mg, 80%). MS (CI/NH3) m/z 335 (M+H)+. 1H NMR (CDCl3, 300 MHz) δ 1.65-2.10 (m, 6H), 2.26-2.37 (m, 1H), 2.41-2.47 (m, 2H), 2.48 (s, 3H), 2.61-2.73 (m, 1H), 2.76-2.83 (m, 2H), 3.07-3.16 (m, 1H), 3.89-4.03 (m, 2H), 7.17-7.36 (m, 6H), 8.21-8.26 (m, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06127386
출처 데이터셋uspto-grants-2000_10
ORD IDord-4a2de69c00024767af48f4f633003dea
출처 메모uspto-grants-2000_10