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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35244Generated: October 30, 2026

Hydrogen Bromide → N-(4-aminophenethyl)-1,2,3,4-tetrahydro-6,7-dihydroxy-1-methylisoquinoline dihydrobromide

https://huagongshe.com/reaction/35244

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantVeradoline HydrochlorideHCID 3033629—
ProductN-(4-aminophenethyl)-1,2,3,4-tetrahydro-6,7-dihydroxy-1-methylisoquinoline dihydrobromideHCID 14230315—

Reaction Steps

N-(4-Aminophenethyl)-1,2,3,4-tetrahydro-6,7-dimethoxy-1-methylisoquinoline dihydrochloride (10.0 g, 0.025 m) was dissolved in 49% HBr (25 ml) maintained under nitrogen and heated to 120° for 18 hr. after which time a white solid had precipitated. The mixture was cooled and the solid slurried with isopropanol (50 ml), stirred for 1 hr., and the solid collected by filtration. The solid was washed three times with isopropanol and vacuum dried at 100° for 48 hr. to give 8.5 g N-(4-aminophenethyl)-1,2,3,4-tetrahydro-6,7-dihydroxy-1-methylisoquinoline dihydrobromide as an off-white solid, m.p. 275°-278°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04766131
Source datasetuspto-grants-1988_08
ORD IDord-927e402d66544e428ea75208f97b14a0
Source noteuspto-grants-1988_08