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1037-20-3

1-(2-phenoxyethyl)-4-phenyl-piperazine synthesis

9synthesis methods
-

Yield:1037-20-3 97%

Reaction Conditions:

with lithium carbonate in acetonitrile; for 24 h;Reflux;Inert atmosphere;

Steps:

4.1.7. General procedure for preparation of functionalized N-phenylpiperazine derivatives (7a-b), (7d-k), (8a-b) and (8d-f)

General procedure: To a suspension of corresponding mesylate derivative (13A-B), (16A-B), (18A-B), (20A-B), (24A-B) (0.50 mmol) and lithium carbonate (0.07 g, 1.00 mmol) in acetonitrile (6 mL), was added the adequate N-phenylpiperazine derivative (2.00 mmol). The mixture was kept at reflux for 24 h under vigorous agitation and nitrogen atmosphere. At the end of this time the solution was concentrated in a rotatory evaporator, solubilized in dichloromethane and mixed with silica gel. The material was separated by chromatography on silica gel eluted with dichloromethane, followed by chloroform to give the desired N-phenylpiperazine derivatives of 1,3-benzodioxolyl (7) and phenyl (8) series, as described next.

References:

Romeiro, Luiz A.S.;Da Silva Ferreira, Marcos;Da Silva, Leandro L.;Castro, Helena C.;Miranda, Ana L.P.;Silva, Cláudia L.M.;No?l, Franois;Nascimento, Jéssica B.;Araújo, Claudia V.;Tibiri?á, Eduardo;Barreiro, Eliezer J.;Fraga, Carlos A.M. [European Journal of Medicinal Chemistry,2011,vol. 46,# 7,p. 3000 - 3012] Location in patent:experimental part