HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloride methanol → N-(5-Isoquinolyl)ethylenediamine hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloride methanol | HCID 21893726 | — |
| Reactant | N-(tert-butoxycarbonyl)-N'-(5-isoquinolyl)ethylenediamine | HCID 21979917 | — |
| Product | N-(5-Isoquinolyl)ethylenediamine hydrochloride | HCID 21979755 | — |
Reaction Steps
According to the method of Example 1, Step C, deprotection was performed (50° C., 2 hours) by using Intermediate 27 (287 mg) and 10% hydrogen chloride/methanol solution (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 (1 ml) and diethyl ether (3 ml). The deposited precipitates were collected by filtration and washed with diethyl ether to obtain the title compound (252 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-83ccd6a730cf4a3f904464d1133a0cd4 |
| Source note | uspto-grants-2006_08 |