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5-Amino-2-hydroxybenzimidazole → 2-Oxo-N-(2-oxo-2,3-dihydro-1H-benzimidazol-6-yl)-2-(4-p-tolyloxy-piperidin-1-yl)-acetamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 5-Amino-2-hydroxybenzimidazole | HCID 66765 | — |
| 反応物 | Oxo-(4-p-tolyloxy-piperidin-1-yl)-acetic acid | HCID 69100252 | — |
| 生成物 | 2-Oxo-N-(2-oxo-2,3-dihydro-1H-benzimidazol-6-yl)-2-(4-p-tolyloxy-piperidin-1-yl)-acetamide | HCID 10200650 | — |
反応手順
The title compound is prepared from oxo-(4-p-tolyloxy-piperidin-1-yl)-acetic acid (Example 26b) and 5-amino-1,3-dihydro-benzimidazol-2-one according to the method described in Example 2. The filtered crystals are purified by column chromatography using Kieselgel 60 (Merck) as adsorbent and toluene:methanol=4:1 as eluent. Melting Point: 294° C. (isopropanol)
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07435744B2 |
| 出典データセット | uspto-grants-2008_10 |
| ORD ID | ord-51dff2f588f14f02843a66f108ba7efb |
| 出典メモ | uspto-grants-2008_10 |