化工社化工社 化学情報印刷レポート · 研究参考用
phenylalaninol, (S)- → (S)-N-[1-benzyl-2-hydroxyethyl]-4-hydroxy-1-methyl-1H-indole-2-carboxamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | phenylalaninol, (S)- | HCID 447213 | — |
| 反応物 | 4-Benzyloxy-1-methyl-1H-indole-2-carbonyl chloride | HCID 22054872 | — |
| 生成物 | (S)-N-[1-benzyl-2-hydroxyethyl]-4-hydroxy-1-methyl-1H-indole-2-carboxamide | HCID 69272852 | — |
| 生成物 | (S)-N-[1-benzyl-2-hydroxyethyl]-4-(benzyloxy)-1-methyl-1H-indole-2-carboxamide | HCID 69276702 | — |
反応手順
From (S)-2-amino-3-phenylpropan-1-ol and 4-benzyloxy-1-methyl-1H-indole-2-carbonyl chloride the intermediate compound (S)-N-[1-benzyl-2-hydroxyethyl]-4-(benzyloxy)-1-methyl-1H-indole-2-carboxamide was prepared by a method analogous to that described in Example 23. MS ES (M++H)=415. Hydrogenation of this intermediate by a method analogous to that described in Example 9 gave the title compound. MS ES (M++H)=325.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07064143B1 |
| 出典データセット | uspto-grants-2006_06 |
| ORD ID | ord-6bb9a43d536b46ce973f4a40981662f4 |
| 出典メモ | uspto-grants-2006_06 |