HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383273Generated: November 1, 2026
Potassium Hydroxide → HCID 25261751, compound
https://huagongshe.com/reaction/383273
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 25261426 | HCID 25261426 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | HCID 25261751 | HCID 25261751 | — |
Reaction Steps
5-[3-(3-pyrazol-1-yl-phenyl)-imidazo-[1,2-a]-pyridin-7-yl]-nicotinonitrile (Ex. 1.8) (1 eq, 0.099 mmol, 40 mg) and potassium hydroxide (10 eq, 0.99 mmol, 64.8 mg) are dissolved in tBuOH (2 ml) and the reaction mixture is heated at 85° C. for 1.5 h. At the completion of this time the solvent is removed in vacuo and the reaction mixture is diluted with NaHCO3. The aqueous phase is extracted with EtOAc. The organic layer is washed with brine, dried over MgSO4, filtered and evaporated to dryness. The reaction mixture is purified by flash chromatography on silica eluting with DCM/MeOH 9/1 to yield 5-[3-(3-pyrazol-1-yl-phenyl)-imidazo-[1,2-a]pyridin-7-yl]-nicotinamide as a yellow solid; [M+H]+=381
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08367662B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-11564801b0eb4e25b9d83a41fc767a24 |
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| Source note | uspto-grants-2013_02 |
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