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HRID 129518作成日:2026年10月27日

Bis(trimethylsilyl)acetylene → N-Methyl-2-(trimethylsilyl)-1H-indole-5-acetamide

https://huagongshe.com/reaction/129518

反応式

関与物質

役割名称HCID仕込み量
反応物Bis(trimethylsilyl)acetyleneHCID 84564—
反応物Sodium BicarbonateHCID 516892—
反応物4-Amino-3-iodo-n-methylbenzeneacetamideHCID 23365810—
溶媒AcetonitrileHCID 6342—
生成物N-Methyl-2-(trimethylsilyl)-1H-indole-5-acetamideHCID 5375441838.8%

反応手順

4-Amino-3-iodo-N-methyl-benzeneacetamide (7) (7.26 g, 0.025 mol), bis(trimethylsilyl) acetylene (8.52 g, 0.05 mol) and tetrakistriphenylphosphine Pd(O) (2.89 g, 0.0025 mol) were dissolved in CH3CN (400 mL) followed by the addition of saturated aqueous NaHCO3 (30 mL). The mixture was heated at reflux for 24 h. The solvent was removed in vacuo and the residue was dissolved in EtOAc. The organic phase was extracted with brine, dried over MgSO4, filtered and concentrated in vacuo. Silica gel chromatography (50-100% EtOAc gradient in hexane) of the concentrate afforded the product (8) (2.52 g, 38.8%) as a yellow viscous oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05468768
出典データセットuspto-grants-1995_11
ORD IDord-742de573106d4029966a3458d1fc3e2c
出典メモuspto-grants-1995_11