【药物名称】PK-9084
化学结构式(Chemical Structure):
参考文献No.47468
标题:1-(4 Quinolyl) 2- or 3- (2- or 3- piperidyl or pyrrolidinyl) ethanone or propanone, process for their preparation and their use as medicaments
作者:Dubroeucq, M.C.; Gueremy, C.G.A.; Lefur, G.R.; Mizoule, J. (Pharmindustrie)
来源:EP 0042781
合成路线图解说明:

The reaction of ethyl 2-phenylquinoline-4-carboxylate (I) with N-benzoylpipepidine-3-acetic acid ethyl ester (II) by means of potassium hydride in THF gives 2-phenyl-4-[2-(3-piperidyl)acetyl]quinoline (III), which is reduced with hydrazine in dietyleneglycol at 180 C.

参考文献No.71695
标题:PK-8165 and PK-9084
作者:Blancafort, P.; McGillion, F.B.; Casta馿r, J.; Serradell, M.N.
来源:Drugs Fut 1982,7(9),648
合成路线图解说明:

The reaction of ethyl 2-phenylquinoline-4-carboxylate (I) with ethyl N-benzoylpiperidyl-4-acetate (II) by means of potassium tert-butylate in THF gives 2-phenyl-4-(4-piperidylacetyl)quinone (III), which is then reduced with hydrazine at 180 C.

合成路线图解说明:

The reaction of ethyl 2-phenylquinoline-4-carboxylate (I) with N-benzoylpipepidine-3-acetic acid ethyl ester (II) by means of potassium hydride in THF gives 2-phenyl-4-[2-(3-piperidyl)acetyl]quinoline (III), which is reduced with hydrazine in dietyleneglycol at 180 C.

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