HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2039773Generated: October 29, 2026
Acetyl chloride → 4-Hydroxymethylpyrazolo[1,5-a]pyridine-2-carboxylic acid ethyl ester
https://huagongshe.com/reaction/2039773
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-Hydroxymethylpyrazolo[1,5-a]pyridine-2-carboxylic acid | HCID 67113591 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Hydroxymethylpyrazolo[1,5-a]pyridine-2-carboxylic acid ethyl ester | HCID 59538960 | — |
Reaction Steps
Acetyl chloride (9.5 mL, 130 mmol) is added to absolute ethanol (200 mL). After 30 min, the solution is poured into the flask containing 4-hydroxymethyl-pyrazolo[1,5-a]pyridine-2-carboxylic acid. The mixture is warmed to 50° C. for 3.5 h. After cooling to rt, the mixture is made basic with dropwise addition of sat. aq. NaHCO3. The volatiles are removed under reduced pressure. The aqueous solution is extracted with EtOAc. The organics are dried over Na2SO4, filtered, and concentrated to afford the title compound as a tan powder. LC-MS m/z (M+Na+): 242.98§.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08580812B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-5d961a3c22bc4fd7a130f57abc642c19 |
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| Source note | uspto-grants-2013_11 |
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