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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant3-Chloro-2-hydrazinylpyridineHCID 556100—
ReactantMethyl 2-bromo-4-chloro4-oxobutanoateHCID 11390578—
ReactantHCID 178514363HCID 178514363—
SolventAcetonitrileHCID 6342—
ProductMethyl 2-(3-Chloro-2-pyridyl)-5-oxopyrazolidine-3-carboxylateHCID 1142536489.8%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834186B2
Source datasetuspto-grants-2010_11
ORD IDord-11305372bf98425c9c27647b6be38084
Source noteuspto-grants-2010_11