Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 67238887 | HCID 67238887 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 67425102 | HCID 67425102 | 90% |
Reaction Steps
1 g of the (6S)-(−)-5,6,7,8-tetrahydro-6-[propyl-(2-thienyl)ethyl]amino-1-naphthol (I) obtained in Example 3 (96.58% purity by HPLC) was dissolved in 8 mL of ethyl acetate at room temperature. Then, 1.5 mL of 2.5M HCl solution was added in isopropanol. The mixture was cooled for 3 hours at 0-5° C. and a white solid precipitated. The mixture was filtered off to afford 1 g of (6S)-(−)-5,6,7,8-tetrahydro-6-[propyl-(2-thienyl)ethyl]amino-1-naphthol hydrochloride (90% yield). The product was analyzed by HPLC and its purity was 98.58%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08513438B2 |
|---|
| Source dataset | uspto-grants-2013_08 |
|---|
| ORD ID | ord-abcb642dab384b499fd69a634a545e4f |
|---|
| Source note | uspto-grants-2013_08 |
|---|