HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → HCID 24960989, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 4741833 | HCID 4741833 | — |
| Reactant | Daidzein | HCID 5281708 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 24960989 | HCID 24960989 | — |
Reaction Steps
To a solution of 1-[4-(2-chloroethyl)piperazinyl]-4-methoxybenzene (0.929 mmol) and 4,7-dihydroxyisoflavone (0,929 mmol) in acetone (10 ml)was added 11% potassium hydroxide (0.5 ml), and the mixture stirred at reflux temperature for 48 hours. Sufficient methanol was added to precipitate unreacted starting material, which was filtered off, and solvent was removed from the filtrate under reduced pressure. The residue was purified by biotage column chromatography, eluting with 5% methanol/methylene chloride, to provide pure 3-(4-hydroxyphenyl)-7-{2-[4-(4-methoxyphenyl)piperazinyl]ethoxy}chromen-4-one.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08158810B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-61cc0cbe325b4f5580cb7d283ad44eaf |
| Source note | uspto-grants-2012_04 |