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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1521990Generated: October 29, 2026

Sodium Bicarbonate → HCID 67003597, compound

https://huagongshe.com/reaction/1521990

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantTert-butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2,3,6-tetrahydropyridine-1-carboxylateHCID 4642098—
ReactantHCID 67003641HCID 67003641—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 67003597HCID 67003597—

Reaction Conditions

Temperature72 °C

Reaction Steps

A mixture of Example 229B (0.808 g, 1.730 mmol), tert-butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-5,6-dihydropyridine-1(2H)-carboxylate (Frontier Scientific, 0.588 g, 1.903 mmol) and sodium hydrogencarbonate (0.436 g, 5.19 mmol) in degassed N,N-dimethylformamide (10.81 mL) and water (3.6 mL) was treated with bis(triphenylphosphine)palladium(II) chloride (0.121 g, 0.173 mmol) under nitrogen and the mixture was heated at 72° C. for 24 hours. The mixture was cooled to ambient temperature, suspended in 80 mL water, stirred for 30 minutes and filtered. Purification by flash chromatography on silica gel (AnaLogix IntelliFlash 280) eluting with a gradient of 0-20% ethyl acetate in hexanes afforded the title compound. MS (ESI+) m/z 522.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073922B2
Source datasetuspto-grants-2015_07
ORD IDord-d77fa5da1792454ebad18aa8a06d3ab5
Source noteuspto-grants-2015_07