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Tetrahydrofuran → N-cyclohexylmethyl-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 | Cyclohexanemethylamine | HCID 76688 | — |
| 反応物 | 3-Methoxy-4-(2-propynyloxy)benzoyl chloride | HCID 57445671 | — |
| 溶媒 | Triethylamine | HCID 8471 | — |
| 生成物 | N-cyclohexylmethyl-4-(2-propynyloxy)-3-methoxybenzamide | HCID 57445682 | 82% |
反応手順
To a mixture of 10 ml of THF and 0.20 g of 3-methoxy-4-(2-propynyloxy)benzoyl chloride were added dropwise 0.22 g of cyclohexylmethylamine and 0.20 g of triethylamine in order under ice cooling The mixture obtained was stirred at room temperature for 4 hours. Then, the reaction mixture was concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to obtain 0.22 g of N-cyclohexylmethyl-4-(2-propynyloxy)-3-methoxybenzamide (hereinafter, described as the compound 17 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-9cd950a9440c48c49d51b3c206f62b4d |
| 出典メモ | uspto-grants-2011_03 |