Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1449133Generated: November 2, 2026

2-(1,2,3,4-Tetrahydroisoquinolin-3-yl)ethan-1-ol → (RS)-3-(2-Hydroxyethyl)-N-(3-methylisoquinol-5-yl)-1,2,3,4-tetrahydroisoquinoline-2-carbothioamide

https://huagongshe.com/reaction/1449133

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(1,2,3,4-Tetrahydroisoquinolin-3-yl)ethan-1-olHCID 12874855—
Reactant5-Isothiocyanato-3-methylisoquinolineHCID 13014321—
SolventEthanolHCID 702—
Product(RS)-3-(2-Hydroxyethyl)-N-(3-methylisoquinol-5-yl)-1,2,3,4-tetrahydroisoquinoline-2-carbothioamideHCID 2035006699.5%

Reaction Conditions

Temperature20 °C

Reaction Steps

5-Isothiocyanato-3-methylisoquinoline (8.8 g) is added to a solution of (RS)-3-(2-hydroxyethyl)-1,2,3,4-tetrahydroisoquinoline (7.8 g) in ethanol (150 cc). A white precipitate rapidly forms. After stirring for 17 hours at a temperature of about 20° C., the mixture is evaporated to dryness at 40° C. under reduced pressure (30 mm Hg). (RS)-3-(2-Hydroxyethyl)-N-(3-methylisoquinol-5-yl)-1,2,3,4-tetrahydroisoquinoline-2-carbothioamide (16.5 g) is thus obtained in the form of pale yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04189480
Source datasetuspto-grants-1980_02
ORD IDord-72f2e82c090f422ca576cc23921a7af2
Source noteuspto-grants-1980_02