HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → 1-(4-Ethylpiperazin-1-yl)-7-methoxy-3-(2-methoxyphenyl)isoquinoline dihydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Ethylpiperazine | HCID 79196 | — |
| Reactant | 1-Chloro-7-methoxy-3-(2-methoxyphenyl)isoquinoline | HCID 22503621 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-(4-Ethylpiperazin-1-yl)-7-methoxy-3-(2-methoxyphenyl)isoquinoline dihydrochloride | HCID 22502928 | — |
Reaction Steps
1-Chloro-7-methoxy-3-(2-methoxyphenyl)isoquinoline (0.56 g) was reacted with N-ethylpiperazine (5 ml) and potassium carbonate (0.5 g) at 120° C. for 5 hr. To the resulting reaction solution were added ethyl acetate and water, and then it was extracted with ethyl acetate. The resulting organic layer was washed with water and brine, and dried over magnesium sulfate. The solvent was evaporated, and the resulting residue was purified by silica gel column chromatography (methylene chloride/methanol system), to give 0.43 g of the free compound of the title compound as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06790844B2 |
| Source dataset | uspto-grants-2004_09 |
| ORD ID | ord-04df4cca83b04b718c6ecb19ded9d024 |
| Source note | uspto-grants-2004_09 |