HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1173543Generated: November 1, 2026
Sodium Bicarbonate → Methyl 2-(3-Chloro-2-pyridyl)-5-oxopyrazolidine-3-carboxylate
https://huagongshe.com/reaction/1173543
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3-Chloro-2-hydrazinylpyridine | HCID 556100 | — |
| Reactant | Methyl 2-bromo-4-chloro4-oxobutanoate | HCID 11390578 | — |
| Reactant | HCID 178514363 | HCID 178514363 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Methyl 2-(3-Chloro-2-pyridyl)-5-oxopyrazolidine-3-carboxylate | HCID 11425364 | 89.8% |
Reaction Steps
The crude product of Step B (i.e. methyl 2-bromo-4-chloro-4-oxobutanoate) (11.00 g, ˜47.4 mmol) in acetonitrile (25 mL) was added over 65 minutes to a mixture of 3-chloro-2(1H)-pyridinone hydrazone (alternatively named (3-chloro-pyridin-2-yl)-hydrazine) (6.55 g, 45.6 mmol) and sodium bicarbonate (9.23 g, 0.110 mol) in acetonitrile (60 mL) at 0° C. The mixture was then allowed to warm to room temperature and was stirred for 3 h. The mixture was then warmed and maintained at 38° C. for 8 h. Then the mixture was allowed to cool, and the solvent was removed by evaporation under reduced pressure. Water (25 mL) was added, and acetic acid (about 1.9 mL) was added until the slurry had a pH of about 5. After 2 h, the product was isolated by filtration, rinsed with water (10 mL) and dried in vacuo to provide the title compound as a pale yellow solid (11 g, 89.8% yield). A sample recrystallized from ethanol melted at 147-148° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07834186B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-11305372bf98425c9c27647b6be38084 |
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| Source note | uspto-grants-2010_11 |
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