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Bis(trimethylsilyl)acetylene → N-Methyl-2-(trimethylsilyl)-1H-indole-5-acetamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Bis(trimethylsilyl)acetylene | HCID 84564 | — |
| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 反応物 | 4-Amino-3-iodo-n-methylbenzeneacetamide | HCID 23365810 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | N-Methyl-2-(trimethylsilyl)-1H-indole-5-acetamide | HCID 53754418 | 38.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05468768 |
| 出典データセット | uspto-grants-1995_11 |
| ORD ID | ord-742de573106d4029966a3458d1fc3e2c |
| 出典メモ | uspto-grants-1995_11 |