化工社化工社 化学情報印刷レポート · 研究参考用
Isopropylamine → 5-Isopropylamino-4-hydroxypentanoic acid
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Isopropylamine | HCID 6363 | — |
| 反応物 | Homoveratrylamine | HCID 8421 | — |
| 反応物 | Chlorolactic acid | HCID 92899 | — |
| 反応物 | 4-Hydroxy-5-chloropentanoic acid | HCID 20240654 | — |
| 生成物 | 5-Isopropylamino-4-hydroxypentanoic acid | HCID 20240650 | — |
反応手順
The procedure is repeated in all essential details, except 4-hydroxy-5-chloropentanoic acid is substituted for β-chlorolactic acid and isopropylamine is substituted for 3,4-dimethoxyphenethylamine to produce the intermediate 5-isopropylamino-4-hydroxypentanoic acid. The hydroxy and amino groups are protected as described in Example I. The resulting acid is reacted with 1-naphthol instead of phenol and the protecting groups are removed as in Example I. The resulting compound should be a short acting β-blocker.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04604481 |
| 出典データセット | uspto-grants-1986_08 |
| ORD ID | ord-14d303843c2a4c13a782419fb3c78137 |
| 出典メモ | uspto-grants-1986_08 |