Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | Thiosemicarbazide | HCID 2723789 | — |
| Reactant | HCID 178434462 | HCID 178434462 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178434443 | HCID 178434443 | — |
Reaction Steps
Sodium acetate (166 mg, 2.02 mmol), thiosemicarbazide (333 mg, 3.66 mmol), 100 ml ethanol and 2 ml distilled water were charged into a 250 ml round bottom flask. The resulting suspension was heated to 80° C. until it becomes a clear solution. The reaction was then cooled down to room temperature and the resulting mixture was added into a 250 ml round bottom flask containing 3-methyl-1H-pyrazolo[3,4-b]pyridine-5-carbaldehyde (333 mg, 2.1 mmol). After the addition, the resulting mixture was heated to 80° C. for 16 hours. The mixture was cooled to room temperature and solid was precipitated out. The solid was filtered off and washed with ether (50 ml). The product (500 mg, y=95%) was used directly for the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07354944B2 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-e20d695cea87441f8cdc6f03f778d7b3 |
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| Source note | uspto-grants-2008_04 |
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