Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1H-indole-2-thiol | HCID 14053212 | — |
| Reactant | HCID 14053214 | HCID 14053214 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 14053215 | HCID 14053215 | 83% |
Reaction Steps
To a solution of 2-mercaptoindole (1.34 g, 8.98 mmol) and 2-chloromethyl-5-methyl-4-piperidinopyridine hydrochloride (2.35 g, 9.00 mmol) in ethanol (90 ml) was added a 2N aqueous sodium hydroxide solution (9.0 ml) under ice-cooling, and the mixture was stirred at room temperature for 30 minutes. After the removal of the organic solvent by evaporation under a reduced pressure, a saturated sodium chloride solution was added to the residue and the mixture was extracted with chloroform. The chloroform layer separated was dried over anhydrous magnesium sulfate and then concentrated in vacuo. The residue was purified by a silica gel column chromatography [eluent: chloroform and then chloroform-methanol (50:1)] whereby to yield the titled compound (2.51 g) as a crystalline substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04743609 |
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| Source dataset | uspto-grants-1988_05 |
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| ORD ID | ord-f572d70d3e4b483d847b8083d5019f7b |
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| Source note | uspto-grants-1988_05 |
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