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Tetrahydrofuran → N-(2-methylcyclopentyl)-3-methoxy-4-(2-propynyloxy)benzamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Tetrahydrofuran | HCID 8028 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 2-Methylcyclopentan-1-amine hydrochloride | HCID 19101439 | — |
| 反応物 | 3-Methoxy-4-(2-propynyloxy)benzoyl chloride | HCID 57445671 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | N-(2-methylcyclopentyl)-3-methoxy-4-(2-propynyloxy)benzamide | HCID 57445683 | 36.7% |
反応手順
To a mixture of 20 ml of THF, 0.50 g of 2-methylcyclopentylamine hydrochloride and 1.0 g of triethylamine was added 0.50 g of 3-methoxy-4-(2-propynyloxy)benzoyl chloride. The mixture obtained was stirred at room temperature for 3 hours. Then, water was added to the reaction mixture and the mixture was extracted with ethyl acetate. The organic layer was dried and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to obtain 235 mg of N-(2-methylcyclopentyl)-3-methoxy-4-(2-propynyloxy)benzamide (hereinafter, described as the compound 18 of the present invention) represented by the formula:
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07902400B2 |
| 出典データセット | uspto-grants-2011_03 |
| ORD ID | ord-1bf4ea1c1e584c7eb2436317bd392241 |
| 出典メモ | uspto-grants-2011_03 |