HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → Hydrogen maleate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Maleic Acid | HCID 444266 | — |
| Reactant | 1-(3-Isopropyl-2-phenyl-5-oxazolidinylmethoxy)-7-methoxyisoquinoline | HCID 20369801 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Hydrogen maleate | HCID 11966254 | — |
| Product | 1-(2-Hydroxy-3-isopropylaminopropoxy)-7-methoxyisoquinoline | HCID 20369794 | — |
Reaction Steps
1 g of 1-(3-isopropyl-2-phenyl-5-oxazolidinylmethoxy)-7-methoxy-isoquinoline is heated to 80° in 10 cc of 1 N hydrochloric acid for 10 minutes. The reaction mixture is extracted with ether. The ethereal phase is discarded, and the aqueous phase is made alkaline with potash, extracted with ether, the ether phase is dried over magnesium sulphate and concentrated, whereby a crystalline product is obtained which is treated in methanol with maleic acid. Ether is added, whereby 1-(2-hydroxy-3-isopropylaminopropoxy)-7-methoxyisoquinoline is obtained as hydrogen maleate. M.P. 144°-146°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04073909 |
| Source dataset | uspto-grants-1978_02 |
| ORD ID | ord-82a2a7a4b92e470e809f317db19c9646 |
| Source note | uspto-grants-1978_02 |