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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 657Generated: October 28, 2026

(S)-1,2-Dimethylpiperazine → HCID 135566983, compound

https://huagongshe.com/reaction/657

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-1,2-DimethylpiperazineHCID 28305740—
ReactantHCID 178418188HCID 178418188—
ReagentSodium t-butoxideHCID 23676156—
Catalyst2-Dicyclohexylphosphino-2',6'-diisopropoxybiphenylHCID 16217985—
CatalystHCID 66572931HCID 66572931—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 135566983HCID 13556698334.73%

Reaction Conditions

Temperature115 °C

Reaction Steps

A mixture of CHLORO(2-DICYCLOHEXYLPHOSPHINO-2',6'-DI-I- PROPOXY-1,1'-BIPHENYL)[2-(2-AMINOETHYLPHENYL)]PALLADIUM(II), METHYL-T- BUTYLETHER ADDUCT (Ru Phos Pd cycle) (69.2 mgs, 0.2eq), sodium tert-butoxide (244 mg, 2.54 mmol) ,2-(4-(6-chloro-4-methylpyridin-3-yl)phenyl)-8-(hydroxymethyl)quinazolin-4(3H)-one (200 mg, 0.42 mmol) , (S)-1,2-dimethylpiperazine (198 mg, 1.06 mmol) in dioxane (20ml) was stirred at 115°C for 1hr, LCMS indicated the completion of reaction. The solid was filtered off through a pad of celite, washed with DCM. The solvent of the filtrate was removed by concentration, taken into 2ml of DMSO, purified with reverse phase chromatography column (eluted with 5% to 50% 0.1%TFA in ACN/0.1%TFA in water), the fractions were combined and lyphlized, to yield 117mgs of product. LCMS indicated 9% of TFA coupled side product. The solid was taken into 10ml sat. NaHCO3 aq, sonicated, until the disapearance of the side product, filtered, washed with water, dried to yield (S)-2-(4-(6-(3,4-dimethylpiperazin-1-yl)-4-methylpyridin-3-yl)phenyl)-8-(hydroxymethyl)quinazolin-4(3H)-one (67.0 mg, 34.7 %) as a yellow solid.

Provenance & Evidence

Source dataset750 AstraZeneca ELN dataset
ORD IDord-135c33d2da2b4d7f90276e4b49e654c9
Source note750 AstraZeneca ELN dataset