Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 59700605 | HCID 59700605 | — |
| Product | HCID 10474077 | HCID 10474077 | 94% |
Reaction Steps
Add sodium hydride (25.5 mg, 0.64 mmol) to a solution of 4-[2-(6-chloro-pyridin-2-yl)-pyrazolo[1,5-a]pyridin-3-yl]-quinoline (50 mg, 0.14 mmol) in ethanol (2.5 mL) at 0° C. Stir the reaction mixture at 0° C. for 10 minutes, room temperature for 10 minutes more, and reflux overnight. Cool the reaction mixture to room temperature, quench with saturated aqueous ammonium chloride (3 mL). Add water (20 mL) and extract the aqueous solution with methylene chloride (3×20 mL). Dry the combined organic layers with sodium sulfate and purify by flash column chromatography (SiO2, 50% ethyl acetate/hexanes) to give the title compound 48 mg (94%) as an off-white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07365066B2 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-f9ae9965496e4de29fa7f26c49e90d79 |
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| Source note | uspto-grants-2008_04 |
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