HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 19894546, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 19894535 | HCID 19894535 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 19894546 | HCID 19894546 | — |
Reaction Steps
A solution of 1-[[6-(acetyloxy)-3,4-dihydro-2,5,7,8-tetramethyl-2H-1-benzopyran-2-yl]acetyl]-4-[3-(ethylamino)-2-pyridinyl]-piperazine (EXAMPLE 68, 0.80 g) in methanol (20 ml) is mixed with potassium carbonate (10% aqueous, 1.5 ml) and stirred for 3.5 hr at 20°-25° under a nitrogen atmosphere. Then acetic acid (0.2 ml) is added and the solution is concentrated. The residue is partitioned between methylene chloride and potassium bicarbonate (1N). The organic extracts are combined and washed with water, dried over magnesium sulfate and concentrated to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05120843 |
| Source dataset | uspto-grants-1992_06 |
| ORD ID | ord-a4ccfe3f67ba49d481052db7b7c9f329 |
| Source note | uspto-grants-1992_06 |