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Tetrahydrofuran → N-cyclopentylmethyl-4-(2-propynyloxy)-3-methoxybenzamide
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 | Cyclopentanemethylamine | HCID 80153 | — |
| 反応物 | 3-Methoxy-4-(2-propynyloxy)benzoyl chloride | HCID 57445671 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | N-cyclopentylmethyl-4-(2-propynyloxy)-3-methoxybenzamide | HCID 57445678 | 80.8% |
反応手順
To a mixture of 10 ml of THF and 0.3 g of 3-methoxy-4-(2-propynyloxy)benzoyl chloride were added dropwise 0.15 g of cyclopentylmethylamine and 0.16 g of triethylamine in order under ice cooling. The mixture obtained was stirred at room temperature for 4 hours. Then, ethyl acetate was added to the reaction mixture and it was filtered through Celite. The filtrate was concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to obtain 0.31 g of N-cyclopentylmethyl-4-(2-propynyloxy)-3-methoxybenzamide (hereinafter, described as the compound 11 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-37742500bdce49d4a45de9a444813b7b |
| 出典メモ | uspto-grants-2011_03 |