HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloride methanol → N-(5-Isoquinolyl)-pentamethylenediamine hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloride methanol | HCID 21893726 | — |
| Reactant | N-(tert-butoxycarbonyl)-N'-(5-isoquinolyl)-pentamethylenediamine | HCID 21979906 | — |
| Product | N-(5-Isoquinolyl)-pentamethylenediamine hydrochloride | HCID 21979922 | — |
Reaction Steps
According to the method of the above Example, deprotection was performed (room temperature, 31 hours) by using Intermediate 31 (327 mg) and 10% hydrogen chloride/methanol solution (5 ml). The solvent was evaporated under reduced pressure, and the residue was added with methanol (1 ml) and diethyl ether (3 ml). The deposited precipitates were collected by filtration and washed with diethyl ether to obtain the title compound (262 mg) as light yellow powdery solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07094789B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-95aa8b8184824c4f92502d147d13a2fb |
| Source note | uspto-grants-2006_08 |