Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Glyoxal | HCID 7860 | — |
| Reactant | HCID 14685792 | HCID 14685792 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 15053320 | HCID 15053320 | — |
Reaction Steps
To a solution of 1-ethyl-4-methylamino-8-(2-benzimidazolyl)thiomethyl-1,2,3,4-tetrahydroquinoline (900 mg) in methanol (20 ml) was added glyoxal (10 ml) and the mixture was stirred for 3 hours at room temperature. The solvent was distilled off and the resulting residue was dissolved in methanol, and to this mixture was added gradually sodium borohydride (1 g). After stirring the mixture for 1 hour at room temperature, the reaction mixture was concentrated. The resulting residue was extracted with dichloromethane and dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent was purified by silica gel column chromatography [eluent:dichloromethane-methanol (99:1)] to give 1-ethyl-4-[N-methyl-N-(2-hydroxyethyl)amino]-8-(2-benzimidazolyl)thiomethyl-1,2,3,4-tetrahydroquinoline (510 mg).
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-78833fa7cc8c496ba159734ca7c3f35a |
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| Source note | uspto-grants-1990_10 |
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