HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 703969Generated: October 25, 2026
Ethyl chloroformate → 3-(3-Methylpyridazin-4-yl)-2-phenylpyrazolo[1,5-a]pyridine
https://huagongshe.com/reaction/703969
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | 3-Methylpyridazine | HCID 74208 | — |
| Reactant | 2-Phenylpyrazolo[1,5-a]pyridine | HCID 15620342 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(3-Methylpyridazin-4-yl)-2-phenylpyrazolo[1,5-a]pyridine | HCID 15158108 | 32% |
Reaction Steps
To a mixture of 2-phenylpyrazolo[1,5-a]pyridine (5.00 g), 3-methylpyridazine (2.90 g) and methylene chloride (20 ml), was added a solution of ethyl chloroformate (5.57 g) in methylene chloride for 17 minutes under ice-cooling and stirred for an hour at the same temperature and then for 6 hours and 40 minutes at room temperature. To the reaction mixture was added methylene chloride (20 ml), and washed with a solution of potassium carbonate (10 ml) and a saturated aqueous solution of sodium chloride (10 ml) and dried over magnesium sulfate. The solvent was removed and chromatographed on silica gel (70 g) with a mixture of n-hexane and ethyl acetate (2:1). The fractions containing the object compound were combined and evaporated in vacuo and recrystallized from a mixture of ethyl acetate and n-hexane to give 3-(3-methylpyridazin-4-yl)-2-phenylpyrazolo[1,5-a]pyridine (2.36 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04985444 |
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| Source dataset | uspto-grants-1991_01 |
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| ORD ID | ord-1b8fad8c32fd46e18cdac9cda1d9d6a2 |
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| Source note | uspto-grants-1991_01 |
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