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Trimethylsilylacetylene → 5-(1-Hydroxy-1-methylethyl)-2-[(trimethylsilyl)ethynyl]pyridine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Trimethylsilylacetylene | HCID 66111 | — |
| 反応物 | 3-Hydroxy-3-phenyl-1-butyne | HCID 92098 | — |
| 反応物 | 1-(3-bromophenyl)-N-isopropyl-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxamide | HCID 12991318 | — |
| 反応物 | 2-(6-Bromo-3-pyridyl)-2-propanol | HCID 22391973 | — |
| 生成物 | 5-(1-Hydroxy-1-methylethyl)-2-[(trimethylsilyl)ethynyl]pyridine | HCID 22714299 | — |
反応手順
Following the procedure of EXAMPLE 15, but substituting the product 2-bromo-5-(1-hydroxy-1-methylethyl)pyridine from present Step 1 for N-isopropyl-1-(3-bromophenyl)-1,4-dihydro[1,8]naphthyridin-4-one-3-carboxamide and trimethylsilylacetylene for 2-phenyl-3-butyn-2-ol, the 5-(1-hydroxy-1-methylethyl)-2-[(trimethylsilyl)ethynyl]pyridine compound was obtained.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06743802B2 |
| 出典データセット | uspto-grants-2004_06 |
| ORD ID | ord-822a8419b4af419f81bb282333b1a4ee |
| 出典メモ | uspto-grants-2004_06 |