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Tetrahydrofuran → N-(2-methylcyclohexyl)-3,5-dimethoxy-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-Methylcyclohexylamine | HCID 23432 | — |
| 反応物 | 3,5-Dimethoxy-4-(2-propynyloxy)benzoyl chloride | HCID 57445669 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | N-(2-methylcyclohexyl)-3,5-dimethoxy-4-(2-propynyloxy)benzamide | HCID 57701169 | 83.7% |
反応手順
To a mixture of 15 ml of THF and 0.45 g of 3,5-dimethoxy-4-(2-propynyloxy)benzoyl chloride were added 0.24 g of 2-methylcyclohexylamine and 0.27 g of triethylamine in order at room temperature. The mixture obtained was stirred at room temperature for 4 hours. Then, ethyl acetate was added to the reaction mixture and the mixture was filtered through Celite. The filtrate was concentrated under reduced pressure. The residue obtained was washed with methyl tert-butyl ether and hexane to obtain 0.49 g of N-(2-methylcyclohexyl)-3,5-dimethoxy-4-(2-propynyloxy)benzamide (hereinafter, described as the compound 19 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-b9f4cc769b7e4f7ea4346a039bf97167 |
| 出典メモ | uspto-grants-2011_03 |