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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2375478Generated: October 31, 2026

3,4-Dichloroaniline → HCID 10226296, compound

https://huagongshe.com/reaction/2375478

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-DichloroanilineHCID 7257—
ReactantBinap, (A+-)-HCID 634876—
ReactantHCID 21101361HCID 21101361—
ReactantPotassium tert-butoxideHCID 23665647—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 10226296HCID 1022629665.8%

Reaction Conditions

Temperature110 °C

Reaction Steps

Potassium tert-butoxide (1.6 mmol, 1 M in 2-methyl 2-propanol) was added to a solution of N-[2-(4-benzyl-1-piperazinyl)-6-chloro-4-pyrimidinyl]-N,N-dimethylamine (0.331 g, 0.997 mmol) and 3,4 dichloroaniline (0.178 g, 1.10 mmol) in dioxane (2 mL). Subsequently, tris(dibenzylidineacetone)dipalladium (40 mg, 0.04 mmol) and 2,2′-Bis(diphenylphosphino)-1,1′-binapthyl (44 mg, 0.070 mmol) were added and the mixture was stirred for 7 h at 110° C. The resulting mixture was cooled to room temperature and concentrated under reduced pressure. The residue was treated with saturated NaHCO3 (50 mL) and extracted with CH2Cl2 (3×50 mL). The organic layer washed with brine (2×100 mL), dried over Na2SO4, concentrated in vacuo, and purified by preparative TLC using hexane/EtOAc to give the desired product (300 mg, 65%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07465750B2
Source datasetuspto-grants-2008_12
ORD IDord-0e17b5d5d1094a428ba5460323ec4ffd
Source noteuspto-grants-2008_12