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HRID 365814作成日:2026年10月27日

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

https://huagongshe.com/reaction/365814

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物5-Phenyl-1-pentyneHCID 74573—
反応物Sodium BicarbonateHCID 516892—
反応物HCID 11288721HCID 11288721—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
触媒HCID 178418476HCID 178418476—
溶媒DichloromethaneHCID 6344—
溶媒TriethylamineHCID 8471—
生成物5-(5-Phenyl-1-pentynyl)-3-(1-methyl-2-(s)-pyrrolidinylmethoxy)pyridineHCID 5425894681.9%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06127386
出典データセットuspto-grants-2000_10
ORD IDord-4a2de69c00024767af48f4f633003dea
出典メモuspto-grants-2000_10