HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloride methanol → 3-[(1-Amino-5-isoquinolyl)oxy]propylamine hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloride methanol | HCID 21893726 | — |
| Reactant | N-(tert-butoxycarbonyl)-3-[(1-amino-5-isoquinolyl)oxy]propylamine | HCID 21979977 | — |
| Product | 3-[(1-Amino-5-isoquinolyl)oxy]propylamine hydrochloride | HCID 21979858 | — |
Reaction Steps
According to the method of Example 1, Step C, deprotection was performed (50° C., 2 hours) by using Intermediate 20 (159 mg) and 10% hydrogen chloride/methanol solution (2.5 ml). The reaction mixture was cooled to room temperature, and then the solvent was evaporated under reduced pressure. The residue was added with methanol (0.5 ml) and diethyl ether (1.5 ml). The deposited precipitates were collected by filtration and washed with diethyl ether to obtain the title compound (116 mg) as white powdery solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07094789B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-40b53d9bfdf444818e70852330749f6c |
| Source note | uspto-grants-2006_08 |