HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → HCID 25030339, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 59403551 | HCID 59403551 | — |
| Reactant | HCID 68466104 | HCID 68466104 | — |
| Product | HCID 25030339 | HCID 25030339 | — |
Reaction Steps
reacting the above the N1-[4-chloro-2-(2-chlorobenzoyl)phenyl]-2-piperazinoacetamide compound with (E)-3-[4-(3-bromopropoxy)-3-methoxyphenyl]-1-(4-luorophenyl)-2-propen-1-one or 3-(3-bromopropoxy)-2-phenyl-4H-4-chromenone in acetone in the presence potassium carbonate, under reflux, for a period of about 15 to about 20 hrs, followed by the removal of potassium carbonate by alteration and evaporating the solvent, under vacuum, and purifying the resultant product to obtain N1-[4-chloro-2-(2-chlorobenzoyl)phenyl]-2-[4-(4-4-[(E)-3-(4-fluorophenyl)-3-oxo-1-propenyl]-2-methoxyphenoxy butyl)piperazino]acetamide or N1-[4-chloro-2-(2-chlorobenzoyl)phenyl]-2-(4-3-[(4-oxo-3-phenyl-4H-2-chromenyl)oxy]propylpiperazino)acetamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08394954B2 |
| Source dataset | uspto-grants-2013_03 |
| ORD ID | ord-a052e10d2f5a45f78f2d5904f3cc0ef9 |
| Source note | uspto-grants-2013_03 |