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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-(1,2,3,4-Tetrahydroisoquinolin-3-yl)ethan-1-ol | HCID 12874855 | — |
| Reactant | 5-Isothiocyanato-3-methylisoquinoline | HCID 13014321 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (RS)-3-(2-Hydroxyethyl)-N-(3-methylisoquinol-5-yl)-1,2,3,4-tetrahydroisoquinoline-2-carbothioamide | HCID 20350066 | 99.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04189480 |
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| Source dataset | uspto-grants-1980_02 |
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| ORD ID | ord-72f2e82c090f422ca576cc23921a7af2 |
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| Source note | uspto-grants-1980_02 |
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