Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | HCID 66579017 | HCID 66579017 | — |
| Product | HCID 52950390 | HCID 52950390 | — |
Reaction Steps
A solution of 1-methyl-3-(morpholin-4-ylcarbonyl)-8-nitro-1,4-dihydrothiochromeno[4,3-c]pyrazole (0.084 g, 0.23 mmol) in acetic acid is heated at 100° C. under nitrogen. Hydrogen peroxide 30% in water (0.5 mL, 3.6 mmol, 15 Eq) is added and the reaction mixture is heated for 30 minutes. After 30 minutes, the solvent is removed under reduced pressure. 10% aqueous NaHCO3 is added to the residue. The mixture is stirred for few minutes and then extracted with DCM. The organic layer is concentrated and purified by column chromatography to afford the title compound as a yellow solid. 1H NMR (DMSO-d6, 400 MHz) δ 8.66 (s, 1H), 8.48 (dd, J=8.5 Hz, J=2.3 Hz, 1H), 8.28 (J=11.8 Hz, 1H), 4.96 (s, 2H), 4.33 (s, 3H), 3.94 (brs, 2H), 3.66-3.63 (m, 6H). MS (ESI+): 393.0. HPLC (max plot) 90.8%; Rt 3.08 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09073940B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-c660533a603c409e8ff8ac5cfcf9182b |
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| Source note | uspto-grants-2015_07 |
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