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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 10545Generated: October 29, 2026

Hydrochloride methanol → N-(4-vinyl-5-isoquinolyl)-1,4-cyclohexanediamine hydrochloride

https://huagongshe.com/reaction/10545

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloride methanolHCID 21893726—
ReactantN-(tert-butoxycarbonyl)-N'-(4-vinyl-5-isoquinolyl)-1,4-cyclohexanediamineHCID 21979768—
ProductN-(4-vinyl-5-isoquinolyl)-1,4-cyclohexanediamine hydrochlorideHCID 21979839—

Reaction Steps

According to the method of Example 1, Step C, deprotection was performed (50° C., 2 hours) by using Intermediate 85 (85.5 mg) and 10% hydrogen chloride/methanol solution (2 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 (52.3 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07094789B2
Source datasetuspto-grants-2006_08
ORD IDord-46e100f7ec384b35afcd5adf91303a2d
Source noteuspto-grants-2006_08