HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 436472Generated: October 30, 2026
Hydrogen Sulfide → HCID 12278977, compound
https://huagongshe.com/reaction/436472
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Sulfide | HCID 402 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 8-Quinolinecarbonitrile, 5,6,7,8-tetrahydro-2-phenyl- | HCID 12278975 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 12278977 | HCID 12278977 | — |
Reaction Steps
2-Phenyl-8-cyano-5,6,7,8-tetrahydroquinoline (2 g.) was dissolved in pyridine (5 ml.) and triethylamine (1.3 ml.) and the solution treated with H2S gas for 6 hours and the reaction mixture allowed to stand at room temperature for 12 hours. The solvent was removed and the residual oil dissolved in dilute HCl, extracted with ether (2 × 50 ml.) and the extracts discarded. The aqueous solution was made basic and extracted into chloroform (3 × 50 ml.). The combined extracts were dried and evaporated in vacuo to give 2-phenyl-5,6,7,8-tetrahydroquinoline-8-thiocarboxamide which was dissolved in ethanol (5 ml.), diluted with ether (25 ml.) and the solution saturated with HCl gas. The solvent was removed in vacuo and the residual solid recrystallised from methanol-ether giving hydrochloride of the title compound as colourless needles mpt. 211° C. Found: C, 63.41; H, 5.70; N, 8.94%. C16H16N2S. HCl requires: C, 63.04; H, 5.62; N, 9.19 %.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04009169 |
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| Source dataset | uspto-grants-1977_02 |
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| ORD ID | ord-eee18c7ddc4a4b0892d6461453b90c0a |
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| Source note | uspto-grants-1977_02 |
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