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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2272536Generated: November 2, 2026

Sodium Bicarbonate → Methyl 1-(1-((6-cyclopropyl-2,4'-difluoro-3-isopropoxybiphenyl-4-yl)methyl)piperidin-4-yl)-3-methyl-2-oxo-1,2-dihydropyridine-4-carboxylate hydrochloride

https://huagongshe.com/reaction/2272536

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantSodiumHCID 5360545—
Reactant6-Cyclopropyl-2,4'-difluoro-3-isopropoxybiphenyl-4-carbaldehydeHCID 117992172—
ReactantMethyl 3-methyl-2-oxo-1-(piperidin-4-yl)-1,2-dihydropyridine-4-carboxylate hydrochorideHCID 131733376—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
ProductMethyl 1-(1-((6-cyclopropyl-2,4'-difluoro-3-isopropoxybiphenyl-4-yl)methyl)piperidin-4-yl)-3-methyl-2-oxo-1,2-dihydropyridine-4-carboxylate hydrochlorideHCID 11803773189.7%

Reaction Steps

Triethylamine (35.3 g) was added to a suspension of methyl 3-methyl-2-oxo-1-(piperidin-4-yl)-1,2-dihydropyridine-4-carboxylate hydrochoride (100 g) in THF (2.00 L) at room temperature. After being stirred at the same temperature for 30 minutes, 6-cyclopropyl-2,4′-difluoro-3-isopropoxybiphenyl-4-carbaldehyde (121 g) was added to the reaction mixture. The mixture was stirred at room temperature for 30 minutes. Sodium triacetoxyhydroborate (111 g) and acetic acid (20.9 g) were added to the reaction mixture. The mixture was stirred at room temperature for 16 hours. Aqueous saturated sodium hydrogen carbonate solution (1.30 L) and water (1.30 L) were added to the mixture at room temperature. The mixture was extracted with ethyl acetate (10 L). The organic layer was separated, washed with brine (4.00 L), dried over anhydrous sodium sulfate and concentrated in vacuo. The residue was dissolved in ethyl acetate (1.00 L). 4M hydrogen chloride (ethyl acetate solution, 87 ml) was added to the mixture at room temperature. Then crystalline seeds were added to the mixture. The mixture was diluted with diisopropyl ether (2.00 L) and stirred at room temperature for 1 hour. The precipitate was collected by filtration and washed with diisopropyl ether (1.50 L) to give the title compound (183.7 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120777B2
Source datasetuspto-grants-2015_09
ORD IDord-5427a5d74d354d2696a69785815980f3
Source noteuspto-grants-2015_09