HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1088813Generated: October 29, 2026
Sodium Hydroxide → 8-(5-Methoxy-2-benzimidazolyl)thiomethyl-1-methyl-1,2,3,4-tetrahydroquinoline
https://huagongshe.com/reaction/1088813
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Chloro-5-methoxy-1H-benzimidazole | HCID 519197 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | 1-Methyl-8-chloromethyl-1,2,3,4-tetrahydroquinoline hydrochloride | HCID 22161791 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 8-(5-Methoxy-2-benzimidazolyl)thiomethyl-1-methyl-1,2,3,4-tetrahydroquinoline | HCID 15053332 | 83.1% |
Reaction Steps
5-Methoxy-2-chlorobenzimidazole (0.55 g), thiourea (0.2 g) and ethanol (10 ml) were refluxed for 2 hours. To the reaction mixture was added a solution of 1-methyl-8-chloromethyl-1,2,3,4-tetrahydroquinoline hydrochloride (0.51 g) and sodium hydroxide (0.3 g) in water (5 ml) and the mixture was refluxed for 5 hours. After completion of the reaction, ethanol was distilled off and water was added to the resulting residue, and the mixture was extracted with chloroform. After drying over anhydrous magnesium sulfate, chloroform was distilled off. The resulting residue was purified by silica gel column chromatography [eluent:n-hexane-ethyl acetate (4:1)] to give 8-(5-methoxy-2-benzimidazolyl)thiomethyl-1-methyl-1,2,3,4-tetrahydroquinoline (0.62 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04963566 |
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| Source dataset | uspto-grants-1990_10 |
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| ORD ID | ord-df696adb185e4742983da6ba8101c272 |
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| Source note | uspto-grants-1990_10 |
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