HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 631846Generated: October 30, 2026
Tetrahydrofuran → Methyl 2-(aminocarbonothioyl)-1,2,3,4-tetrahydroisoquinoline-6-carboxylate
https://huagongshe.com/reaction/631846
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Ammonium thiocyanate | HCID 15666 | — |
| Reactant | Methyl 1,2,3,4-tetrahydroisoquinoline-6-carboxylate hydrochloride | HCID 42614607 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Methyl 2-(aminocarbonothioyl)-1,2,3,4-tetrahydroisoquinoline-6-carboxylate | HCID 58147281 | 100.1% |
Reaction Steps
A mixture of ammonium thiocyanate (0.105 g, 1.384 mmol), 6-methoxycarbonyl-1,2,3,4-tetrahydroisoquinoline hydrochloride (0.3 g, 1.3176 mmol) and THF (2 mL) was heated in a CEM microwave reactor for 1 h at 100° C. Upon cooling to room temperature, the reaction mixture was diluted with EtOAc, and washed with H2O, 1 N HCl, saturated aqueous NaHCO3 and brine respectively, dried over anhydrous MgSO4, and concentrated under reduced pressure to afford methyl 2-(aminocarbonothioyl)-1,2,3,4-tetrahydroisoquinoline-6-carboxylate (0.33 g, 47%) as a white solid. LCMS: (FA) ES+251.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09321731B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-babe609544e7486ba413f9cd8ffe4136 |
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| Source note | uspto-grants-2016_04 |
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