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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 629810Generated: November 2, 2026

4-Methoxypiperidine → HCID 117602079, compound

https://huagongshe.com/reaction/629810

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethoxypiperidineHCID 77666—
Reactant5-BromoisoquinolineHCID 736487—
Reactantsodium 2-methylpropan-2-olateHCID 178418730—
CatalystBinap, (A+-)-HCID 634876—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
ProductHCID 117602079HCID 11760207952.4%

Reaction Conditions

Temperature85 °C

Reaction Steps

To 5-bromoisoquinoline (10.40 g, 50 mmol), 4-methoxypiperidine (4.92 mL, 50.0 mmol), Pd2(dba)3 (0.458 g, 0.500 mmol), BINAP (0.934 g, 1.500 mmol), and t-BuONa (6.73 g, 70.0 mmol) was added degassed toluene (60 mL) and the reaction was heated under N2 to 85° C. for 24 h and then to 105° C. for 3 h. The reaction mixture was cooled to ambient temperature and water was added. The phases were separated and the aqueous layer extracted three times with ethyl acetate. The combined organics were washed with brine, dried (Na2SO4), filtered and purified by silica gel chromatography to afford 6.34 g (52.4%) of Intermediate 3A as a pale yellow solid. MS (ESI) m/z: 243.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09315519B2
Source datasetuspto-grants-2016_04
ORD IDord-726ee1b1c78c474c84c7864fb8b65df1
Source noteuspto-grants-2016_04