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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1641441Generated: November 1, 2026

Hydrochloric Acid → HCID 178464833, compound

https://huagongshe.com/reaction/1641441

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2,3-DichloropyridineHCID 16988—
ReactantSodium t-butoxideHCID 23676156—
ReactantN-(4-chloro-2-(1-cyclopropylethylcarbamoyl)phenyl)-5-oxopyrazolidine-3-carboxamideHCID 44185604—
CatalystHCID 178418390HCID 178418390—
Solventtert-ButanolHCID 6386—
ProductHCID 178464833HCID 17846483383.5%

Reaction Steps

To a 2-methyl-2-propanol 3 ml mixed liquid comprising 0.10 g of N-(4-chloro-2-(1-cyclopropylethylcarbamoyl)phenyl)-5-oxopyrazolidine-3-carboxamide and 0.09 g of 2,3-dichloropyridine, 15 wt % of palladium-carbon (DeGussa type E105CA/W, manufactured by Aldrich) was added, and then 0.045 g of sodium t-butoxide was added. The mixed liquid was subjected to reaction under reflux for 9 hours. After the reaction liquid was stood to cool, it was poured to a 1 M HCl aqueous solution, followed by extraction with ethyl acetate. The organic layer was washed with a saturated sodium chloride aqueous solution and dried over anhydrous sodium sulfate. The organic layer was subjected to celite filtration, the filtrate was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=1/0 to 1/1) to obtain 0.11 g of the desired product (melting point: 165 to 167° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08115006B2
Source datasetuspto-grants-2012_02
ORD IDord-c9a0e75b5a004f039b69f3ff979e96ac
Source noteuspto-grants-2012_02