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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1354200Generated: November 2, 2026

Water → HCID 23019677, compound

https://huagongshe.com/reaction/1354200

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantHCID 11489847HCID 11489847—
Reactant2-(Boc-amino)-5-bromopyridineHCID 16217843—
CatalystHCID 178418397HCID 178418397—
CatalystHCID 178418778HCID 178418778—
SolventDimethylformamideHCID 6228—
ProductHCID 23019677HCID 2301967713.3%

Reaction Conditions

Temperature100 °C

Reaction Steps

73 mg of tert-butyl (5-bromopyridin-2-yl)carbamate was dissolved in 1 ml of DMF. 62 mg of silver (I) oxide and 31 mg of tetrakis(triphenylphosphine)palladium were added to the obtained solution, and they were stirred at 100° C. in argon atmosphere for 5 minutes. 1 ml of a solution of 100 mg of ethyl 1-cyclopropyl-9-methyl-4-oxo-8-tributylstannyl-4H-quinolizine-3-carboxylate in DMF was added dropwise to the reaction mixture, and they were stirred at that temperature for 1 hour. The reaction mixture was poured into water. After the extraction with chloroform, the organic layer was washed with water and then dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the obtained residue was purified by the silica gel column chromatography (eluent: hexane/ethyl acetate=1/1) to obtain 11 mg of ethyl 8-(6-tert-butoxycarbonylaminopyridin-3-yl)-1-cyclopropyl-9-methyl-4-oxo-4H-quinolizine-3-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07223773B2
Source datasetuspto-grants-2007_05
ORD IDord-ae9a585711624a31b2ac80d015ed3729
Source noteuspto-grants-2007_05