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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591589Generated: October 30, 2026

HCID 136379399, compound → HCID 136262659, compound

https://huagongshe.com/reaction/591589

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 136379399HCID 136379399—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
SolventEthanolHCID 702—
ProductHCID 136262659HCID 136262659—

Reaction Steps

A solution of tert-butyl 4-(4-(5,7-dimethoxy-4-oxo-3,4-dihydroquinazolin-2-yl)phenyl)-5,6-dihydropyridine-1(2H)-carboxylate (10) (0.34 mmol) in EtOH (10 mL) and HOAc (5 mL) was purged with nitrogen and 10% Pd/C (0.016 g) was added. The mixture was stirred under 1 atmosphere of hydrogen overnight. Then, the solution was filtered through Celite, with MeOH washings, and the filtrate was concentrated in vacuo. The material was purified by flash chromatography on silica gel to afford tert-butyl 4-(4-(5,7-dimethoxy-4-oxo-3,4-dihydroquinazolin-2-yl)phenyl)piperidine-1-carboxylate (11).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238640B2
Source datasetuspto-grants-2016_01
ORD IDord-7ed9140755ee4952918e47f8bbc9f8ee
Source noteuspto-grants-2016_01