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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 10496Generated: October 29, 2026

Hydrochloride methanol → N-[(5-Isoquinolyl)sulfonyl]-N-[2-(phenylsulfonyl)ethyl]-1,3-propylenediamine hydrochloride

https://huagongshe.com/reaction/10496

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloride methanolHCID 21893726—
ReactantN-(tert-butoxycarbonyl)-N'-[(5-isoquinolyl)sulfonyl]-N'-[2-(phenylsulfonyl)ethyl]-1,3-propylenediamineHCID 21979866—
ProductN-[(5-Isoquinolyl)sulfonyl]-N-[2-(phenylsulfonyl)ethyl]-1,3-propylenediamine hydrochlorideHCID 21979859—

Reaction Steps

According to the method of Example 1, Step C, deprotection was performed (50° C., 2 hours) by using Intermediate 9 (266 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 (203 mg) as white powdery solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07094789B2
Source datasetuspto-grants-2006_08
ORD IDord-157b347806e5402d819b7c9214a3f0d4
Source noteuspto-grants-2006_08