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PROCESS FOR THE PREPARATION OF ACETYL-AMIDINIOPHENYLALANYL-CYCLOHEXYLGLYCYL-PYRIDYLALANINAMIDES

机译:乙酰基-亚氨基二苯并丙二酰丙二酰丙二酰丙二胺的制备方法

摘要

The present invention relates to a process for the preparation of acetyl-amidiniophenylalanyl-cyclohexylglycyl-pyridinioalaninamides of the formula I, in which the anions X are physiologically acceptable anions, and their analogs, which are effective inhibitors of the blood coagulation factor Xa and which can be used, for example, for preventing thromboses. The process according to the invention comprises the coupling of 2-[2-acetylamino-3-(4-amidinophenyl)propionylamino]-2-cyclohexylacetic acid, which is obtained from 2-[2-acetylamino-3-(4-cyanophenyl)acryloylamino]-2-cyclohexylacetic acid by asymmetric hydrogenation and conversion of the cyano group into the amidine, or a salt thereof, with a 3-(2-amino-2-carbamoylethyl)-1-methylpyridinium salt or a salt thereof. The invention furthermore provides starting materials and intermediates for this process, processes for their preparation and acetyl-(S)-4-amidiniophenylalanyl-(S)-cyclohexylglycyl-(S)-(1-methyl-3-pyridinio)alaninamide as ditosylate salt.
机译:本发明涉及一种制备式Ⅰ的乙酰-酰胺基苯丙氨酰基-环己基甘氨酰-吡啶基碘丙氨酰胺的方法,其中阴离子X是生理上可接受的阴离子,以及它们的类似物,它们是凝血因子Xa的有效抑制剂并且可以例如,用于预防血栓形成。根据本发明的方法包括由2- [2-乙酰氨基-3-(4-氰基苯基)获得的2- [2-乙酰氨基-3-(4-ami基苯基)丙酰氨基] -2-环己基乙酸的偶联。丙烯酰基氨基] -2-环己基乙酸通过不对称氢化并与3-(2-氨基-2-氨基甲酰基乙基)-1-甲基吡啶盐或其盐将氰基转化为am或其盐。本发明还提供了该方法的起始原料和中间体,其制备方法以及作为二甲苯磺酸盐的乙酰基-(S)-4-酰胺基苯基丙氨酰基-(S)-环己基甘氨酰基-(S)-(1-甲基-3-吡啶基)丙氨酰胺。 。

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