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4-Methoxybenzoic Acid → 2,3-Dihydro-2-[[-(4-methoxybenzoyl)-1-piperazinyl]methyl]-2,4,6,7-tetramethyl-5-benzofuranamine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 4-Methoxybenzoic Acid | HCID 7478 | — |
| 反応物 | 2,3-Dihydro-2,4,6,7-tetramethyl-2-[(1-piperazinyl)methyl]-5-benzofuranamine | HCID 21997779 | — |
| 生成物 | 2,3-Dihydro-2-[[-(4-methoxybenzoyl)-1-piperazinyl]methyl]-2,4,6,7-tetramethyl-5-benzofuranamine | HCID 22110975 | 67% |
反応手順
Using 2,3-dihydro-2,4,6,7-tetramethyl-2-[(1-piperazinyl)methyl]-5-benzofuranamine and p-anisic acid, the procedure of Example 10, presented hereinafter, was otherwise followed to provide the title compound. Yield 67%.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06172085B2 |
| 出典データセット | uspto-grants-2001_01 |
| ORD ID | ord-77a50fbee5354e05ac0f3816662a9eaf |
| 出典メモ | uspto-grants-2001_01 |