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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35243Generated: October 28, 2026

Hydrochloric Acid → HCID 14230313, compound

https://huagongshe.com/reaction/35243

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl EtherHCID 3283—
ReactantVeradoline HydrochlorideHCID 3033629—
SolventHydrogen BromideHCID 260—
SolventMethanolHCID 887—
SolventIsopropanolHCID 3776—
ProductHCID 14230313HCID 14230313—

Reaction Steps

N-(4-Aminophenethyl)-1,2,3,4-tetrahydro-6,7-dimethoxy-1-methylisoquinoline dihydrochloride (20.0 g, 0.05 m) was suspended in 49% HBr (50 ml) maintained under nitrogen and heated to 120° for 1.5 hr. The mixture was cooled and then poured into 500 cc of ice/water and the solution basified to pH 11 and extracted with ether (3×250 ml). The aqueous phase was buffered to pH 8 by adding glacial acetic acid and dilute NaOH as needed, then extracted with chloroform (4×300 ml). The chloroform extracts were dried over MgSO4 and evaporated to an oil, 8.5 g. This crude product was purified by HPLC on silica gel eluting with ammonia saturated 5% CH3OH/CHCl3. Pure fractions were combined and evaporated to give a yellow oil, 5.5 g. This was dissolved in methanol (20 ml) and isopropanol (10 ml), acidified with HCl gas and the stirred solution treated with ether (100 ml). The solid precipitate was collected by filtration, washed with 10% isopropanol/ether and vacuum dried to give N-(4-aminophenethyl)-1,2,3,4-tetrahydro-6-hydroxy-7-methoxy-1-methylisoquinoline dihydrochloride as a white solid, m.p. 201°-205°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04766131
Source datasetuspto-grants-1988_08
ORD IDord-93f46fadcb384f108a04cef5ef4313e1
Source noteuspto-grants-1988_08