Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Sodium Phosphate, Dibasic | HCID 24203 | — |
| Reactant | HCID 19603778 | HCID 19603778 | — |
| Reactant | Sodium hydrogen sulphide | HCID 86586439 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 19603678 | HCID 19603678 | 31.3% |
Reaction Steps
Sodium chloride (19 mg) was added to a mixture of 1-{[2-(4-tert-butylthiazol-2-yl)benzofuran-5-yl]methyl}-5-[3-(ethoxycarbonyl)propoxy]indole-3-carbaldehyde (0.31 g), sodium hydrogenphosphate 12 water (90 mg) and 2-methyl-2-butane (0.27 ml) in a mixed solvent of water (1.5 ml), tetrahydrofuran (2.2 ml) and tert-butanol (6.5 ml). After 2 days, aqueous sodium hydrogensulfide solution was added to the mixture. The resulting mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried over magnesium sulfate and concentrated under reduced pressure. The residue was subjected to column chromatography on silica gel and eluted with a mixture of toluene and ethyl acetate. The fractions containing the objective compound were combined and concentrated under reduced pressure to give 1-{[2-(4-tert-butylthiazol-2-yl)benzofuran-5-yl]methyl}-5-[3-(ethoxycarbonyl)propoxy]indole-3-carboxylic acid (0.10 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05994378 |
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| Source dataset | uspto-grants-1999_11 |
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| ORD ID | ord-09721c8e0a1244748949a723be2df000 |
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| Source note | uspto-grants-1999_11 |
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