HuagongsheHuagongshe Chemistry Print Report · For research reference only
3',4'-Bis(acetoxy)-2-bromoacetophenone → 2-{N-benzyl-N-[2-(2-phenylacetamido)ethyl]amino}-3',4'-bis(acetoxy)acetophenone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3',4'-Bis(acetoxy)-2-bromoacetophenone | HCID 12746020 | — |
| Reactant | N-[2-(benzylamino)ethyl]-2-phenylacetamide | HCID 12876177 | — |
| Product | 2-{N-benzyl-N-[2-(2-phenylacetamido)ethyl]amino}-3',4'-bis(acetoxy)acetophenone | HCID 20446776 | — |
Reaction Steps
3',4'-Bis(acetoxy)-2-bromoacetophenone was reacted with N-[2-(benzylamino)ethyl]-2-phenylacetamide using a similar procedure to that described in Example 1 for the analogous pivaloyloxy derivative to give 2-{N-benzyl-N-[2-(2-phenylacetamido)ethyl]amino}-3',4'-bis(acetoxy)acetophenone, which was isolated as its free base and converted to its hydrochloride salt with ethereal hydrogen chloride to give a solid, m.p. 140°-145° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04423070 |
| Source dataset | uspto-grants-1983_12 |
| ORD ID | ord-3556c4d84089442d906597cfb047b627 |
| Source note | uspto-grants-1983_12 |