Synthesis of heteroaromatic potential. beta.-adrenergic antagonists by the glycidol route

Y Antonio, C Camargo, E Galeazzi…

Index: Antonio,Y. et al. Journal of Medicinal Chemistry, 1978 , vol. 21, p. 123 - 126

Full Text: HTML

Citation Number: 5

Abstract

The synthesis of several 3-alkylamino-2-hydroxypropyl heteroaryl ethers (13-15, 17, and 18) is described. These compounds were prepared by the alkylamination of the corresponding glycidyl ethers (6-8, 10, and ll), which in turn were obtained from the requisite heteroaryl halides and the sodium salt of glycidol. The above basic ethers exhibited@-blocking activity, but the potency of the tested compounds was considerably less than that of propanolol.

Related Articles:

1-Alkylamino-3-(2-thiazolyloxy)-2-propanols. Novel class of mixed myocardial. beta.-stimulants/. beta.-blockers

[Edwards,J.A. et al. Journal of Medicinal Chemistry, 1974 , vol. 17, p. 200 - 203]

1-Alkylamino-3-(2-thiazolyloxy)-2-propanols. Novel class of mixed myocardial. beta.-stimulants/. beta.-blockers

[Edwards,J.A. et al. Journal of Medicinal Chemistry, 1974 , vol. 17, p. 200 - 203]

1-Alkylamino-3-(2-thiazolyloxy)-2-propanols. Novel class of mixed myocardial. beta.-stimulants/. beta.-blockers

[Edwards,J.A. et al. Journal of Medicinal Chemistry, 1974 , vol. 17, p. 200 - 203]

More Articles...