HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isoproterenone hydrochloride → 3-Hydroxy-4-(o-propionamidobenzoyloxy)phenyl isopropylaminomethyl ketone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isoproterenone hydrochloride | HCID 2830496 | — |
| Reactant | o-Propionamidobenzoyl chloride | HCID 20535449 | — |
| Product | 3-Hydroxy-4-(o-propionamidobenzoyloxy)phenyl isopropylaminomethyl ketone | HCID 20535334 | — |
Reaction Steps
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 methanesulfonate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04336400 |
| Source dataset | uspto-grants-1982_06 |
| ORD ID | ord-09785f6008f84b689ff75ff6755bce7a |
| Source note | uspto-grants-1982_06 |