Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Isobutyl iodide | HCID 10556 | — |
| Reactant | Sodium sulfide nonahydrate | HCID 73972 | — |
| Reactant | HCID 10511487 | HCID 10511487 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 68560618 | HCID 68560618 | 41% |
Reaction Steps
An ethanol (14 mL) solution of indolin-5-yl thiocyanate (compound described in the document J. Med. Chem., 1998, vol. 41, p. 1598; 1.33 g, 7.55 mmol) was added to a solution of sodium sulfide nonahydrate (1.84 g, 7.66 mmol) in water (2.8 mL), and the mixture was stirred at 50° C. for 2 hours. To the reaction solution, an ethanol (2.4 mL) solution of isobutyl iodide (1.2 mL, 10.4 mmol) was added, and the mixture was stirred at 50° C. for 2 hours. To the reaction solution, water was added, followed by extraction with ether three times. The obtained organic layer was washed with saturated saline and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane:ethyl acetate=90:10-80:20-55:45, V/V) to obtain the title compound as brown oil (0.65 g, yield: 41%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08232287B2 |
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| Source dataset | uspto-grants-2012_07 |
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| ORD ID | ord-6164950c4d3f48f4aa1a2398d9f824f6 |
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| Source note | uspto-grants-2012_07 |
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