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Trimethylamine → 4-(4-Amino-naphthalen-1-yloxy)-pyrimidine-2-carbonitrile
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Trimethylamine | HCID 1146 | — |
| 反応物 | 4-((2-Chloropyrimidin-4-yl)oxy)naphthalen-1-amine | HCID 22573839 | — |
| 触媒 | Tetraethylammonium cyanide | HCID 3014735 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 4-(4-Amino-naphthalen-1-yloxy)-pyrimidine-2-carbonitrile | HCID 22573833 | 54.1% |
反応手順
To a 0° C. solution of trimethyl amine (20% solution in water, 3.8 mmol) in 2 mL of dimethylformamide was added 4-(2-chloro-pyrimidin-4-yloxy)-naphthalen-1-ylamine (270 mg, 1 mmol). The deep tan solution was warmed to room temperature for 3 h, during which the initially light suspension became a brown suspension. After this time, tetraethylammonium cyanide (156 mg, 1 mmol) was added all at once to provide a deep amber solution. After 1 h, the reaction was quenched with water, extracted with EtOAc and dried over magnesium sulfate. Column chromatography (10-60% EtOAc-hexanes) provided 142 mg (54%) of 4-(4-amino-naphthalen-1-yloxy)-pyrimidine-2-carbonitrile.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06852717B2 |
| 出典データセット | uspto-grants-2005_02 |
| ORD ID | ord-eb0d84ff5d9f4db9b3d85b4257abc054 |
| 出典メモ | uspto-grants-2005_02 |