Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 57901826 | HCID 57901826 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 57901735 | HCID 57901735 | 53% |
Reaction Steps
A mixture of ethyl [(2-{7-[methyl(2-thienylsulfonyl)amino]-1H-indol-2-yl}-1,3-thiazol-5-yl)methoxy]acetate (0.08 g), 1N aqueous sodium hydroxide solution (0.30 mL), tetrahydrofuran (4 mL) and methanol (4 mL) was stirred at 60° C. for 1 hr. The reaction mixture was concentrated, and water was added to the residue. The mixture was acidified with 10% aqueous citric acid solution, and the resulting crystals were filtrated, washed with water, and dried to give the title compound (0.04 g, yield 45%) as pale-yellow crystals. melting point 197-198° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08957070B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-828e2d89c34846d0ac4813bde30b1c11 |
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| Source note | uspto-grants-2015_02 |
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