HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 981960Generated: October 30, 2026
Acetic Anhydride → HCID 53920834, compound
https://huagongshe.com/reaction/981960
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | HCID 53875970 | HCID 53875970 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 53920834 | HCID 53920834 | 62.7% |
Reaction Steps
1-[3-(2-Phenylpyrazolo[1,5-a]pyridin-3-yl)acryloyl]-2-hydroxymethylpiperidine (trans isomer) (0.50 g) was added to a stirred solution of acetic anhydride (0.16 g) in pyridine (5 ml) at room temperature, and stirred at room temperature for 3 hours. Ethyl acetate was added to the reaction mixture and washed with 1N aqueous sodium hydroxide solution, water and saturated sodium chloride aqueous solution, then dried over magnesium sulfate and evaporated in vacuo. The residue was chromatographed on silica gel (50 g) with a mixture of chloroform and acetone (20:1) as an eluent. The fractions containing the objective compound were combined and evaporated in vacuo to give 1-[3-(2-phenylpyrazolo[1,5-a]pyridin-3-yl)acryloyl]-2-acetoxymethylpiperidine (trans isomer) (0.35 g) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04994453 |
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| Source dataset | uspto-grants-1991_02 |
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| ORD ID | ord-7e922e40d29d46a3b4532aab1fe76c63 |
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| Source note | uspto-grants-1991_02 |
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