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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1921158Generated: November 4, 2026

Sodium Carbonate → HCID 67493865, compound

https://huagongshe.com/reaction/1921158

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant1-BenzylpiperazineHCID 75994—
Reactant2-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenylHCID 2734217—
ReactantSodium t-butoxideHCID 23676156—
ReactantHCID 59187099HCID 59187099—
Catalystpalladium(II) acetateHCID 167845—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
ProductHCID 67493865HCID 6749386539.6%

Reaction Conditions

Temperature100 °C

Reaction Steps

0.055 g (0.32 mmol) of 1-benzylpiperazine is introduced into a 50 ml round-bottomed flask under argon comprising 0.036 g (0.37 mmol) of sodium tert-butoxide in solution in 5 ml of toluene through which argon has been bubbled beforehand. 0.06 g (0.29 mmol) of 4-(6-chloropyridin-3-yl)-1-azabicyclo[2.2.1]heptane obtained in stage 5.1 of Example 5, 0.003 g (0.01 mmol) of palladium(II) acetate and 0.011 g (0.03 mmol) of 2-dicyclohexylphosphino-2′-(N,N-dimethylamino)biphenyl are then successively added under an argon atmosphere. The mixture is heated at 100° C. for 3 hours, cooled to ambient temperature, diluted with 40 ml of dichloromethane and poured into 300 ml of a saturated aqueous sodium carbonate solution. The aqueous phase is extracted twice with 100 ml of dichloromethane, and the combined organic phases are dried over sodium sulfate and concentrated under reduced pressure. The residue is purified by chromatography on a column of silica gel, elution being carried out with a mixture of chloroform, methanol and aqueous ammonia in the proportions 90/10/1. 0.04 g of the expected product is obtained in the form of a beige powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173669B2
Source datasetuspto-grants-2012_05
ORD IDord-648d279ffe794c40ba7e33483685743a
Source noteuspto-grants-2012_05