HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isoproterenone hydrochloride → 3-Hydroxy-4-(m-dimethylaminobenzoyloxy)phenyl isopropylaminomethyl ketone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isoproterenone hydrochloride | HCID 2830496 | — |
| Reactant | 3-Dimethylaminobenzoyl chloride | HCID 7010342 | — |
| Product | 3-Hydroxy-4-(m-dimethylaminobenzoyloxy)phenyl isopropylaminomethyl ketone | HCID 53940160 | — |
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 m-dimethylaminobenzoyl chloride instead of isovaleryl chloride, there is obtained 3-hydroxy-4-(m-dimethylaminobenzoyloxy)phenyl isopropylaminomethyl ketone; and by interaction of this base with hydrochloric acid there is obtained the hydrochloride salt. When this hydrochloride is catalytically hydrogenated, using a procedure similar to that described above in Example 2B, there is obtained 3-hydroxy-4-(m-dimethylaminobenzoyloxy)-alpha-(isopropylminomethyl)benzyl alcohol hydrochloride
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04138581 |
| Source dataset | uspto-grants-1979_02 |
| ORD ID | ord-c1c3576927c442f491916bdb003e369b |
| Source note | uspto-grants-1979_02 |