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Isoproterenone hydrochloride → 3-Hydroxy-4-(o-propionamidobenzoyloxy)phenyl isopropylaminomethyl ketone
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Isoproterenone hydrochloride | HCID 2830496 | — |
| 反応物 | o-Propionamidobenzoyl chloride | HCID 20535449 | — |
| 生成物 | 3-Hydroxy-4-(o-propionamidobenzoyloxy)phenyl isopropylaminomethyl ketone | HCID 20535334 | — |
反応手順
Following the procedure described above in Example 58A but using 3,4-dihydroxyphenyl isopropylaminomethyl ketone hydrochloride instead of 3,4-dihydroxyphenyl tert-butylaminomethyl ketone hydrochloride and o-propionamidobenzoyl chloride instead of isovaleryl chloride, there is obtained 3-hydroxy-4-(o-propionamidobenzoyloxy)phenyl isopropylaminomethyl ketone; and by interaction of this base with methanesulfonic acid there is obtained the methanesulfonate salt. When this methanesulfonate is catalytically hydrogenated, using a procedure similar to that described above in Example 2B, there is obtained 3-hydroxy-4-(o-propionamidobenzoyloxy)-alpha-(isopropylaminomethyl)benzyl alcohol and methanesulfonate.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | USRE030241 |
| 出典データセット | uspto-grants-1980_03 |
| ORD ID | ord-443f724e5496481bb85b2a13f9ecf7ef |
| 出典メモ | uspto-grants-1980_03 |