HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466027Generated: October 29, 2026
Sodium Hydroxide → 3-(2-Chloropyridin-4-yl)-2-phenylpyrazolo[1,5-a]pyridine
https://huagongshe.com/reaction/466027
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 3-(2-Oxo-1,2-dihydropyridin-4-yl)-2-phenylpyrazolo[1,5-a]pyridine | HCID 15158112 | — |
| Product | 3-(2-Chloropyridin-4-yl)-2-phenylpyrazolo[1,5-a]pyridine | HCID 15158142 | — |
Reaction Steps
A mixture of 3-(2-oxo-1,2-dihydropyridin-4-yl)-2-phenylpyrazolo[1,5-a]pyridine (0.6 g) and phosphorus oxychloride (1.8 ml) was stirred for 6 hours at 70° C. After cooling, the reaction mixture was poured onto ice (30 g) and made alkaline with 24% aqueous solution of sodium hydroxide (pH=10) and extracted with chloroform (18 ml). The combined extract was washed with water and sodium chloride aqueous solution and dried over magnesium sulfate. The solvent was removed in vacuo and the residue was chromatographed on silica gel (12 g) with chloroform as an eluent. The fractions containing the object compound were combined and evaporated in vacuo and recrystallized from a mixture of ethyl acetate and diisopropyl ether to give 3-(2-chloropyridin-4-yl)-2-phenylpyrazolo[1,5-a]pyridine (0.21 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05155114 |
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| Source dataset | uspto-grants-1992_10 |
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| ORD ID | ord-14eb3298a83749a8bc4fce3859f22e9e |
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| Source note | uspto-grants-1992_10 |
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