首页> 外国专利> A procedure for the preparation of derivatives of 1-amino- (replaced) -3-4'-0-5'-tiazol (replaced) -2-oxi-2-propanol. (Machine-translation by Google Translate, not legally binding)

A procedure for the preparation of derivatives of 1-amino- (replaced) -3-4'-0-5'-tiazol (replaced) -2-oxi-2-propanol. (Machine-translation by Google Translate, not legally binding)

机译:制备1-氨基-(取代的)-3-4'-0-5'-噻唑(取代的)-2-氧代-2-丙醇的衍生物的方法。 (通过Google翻译进行机器翻译,没有法律约束力)

摘要

A process for the preparation of 1-amino (substituted) -3- (4'- or 5'-thiazole (substituted) -2-oxy) -2-propanol derivatives of the formula: **(See formula)** where 2 is a substituent on the thiazole ring at any one of positions 4 or 5, selected from the group of formulas: **(See formula)** where one of the radicals R3 or R4 is independently selected from alkyl of 7 to 12 carbon atoms; cycloalkyl of 3 to 12 carbon atoms; a terminally substituted alkyl group of 2 to 12 carbon atoms, with a substituted terminal carbon atom bearing one to three substituents independently selected from the group consisting of hydroxy, acyloxy of 2 to 12 carbon atoms, and alkoxy of 1 to 6 carbon atoms; and formula groups **(See formula)** where n is an integer from 1 to 4, R8 and R9 are independently selected from the group consisting of hydrogen and alkyl of 1 to 4 carbon atoms and R10 is cycloalkyl of 3 to 8 carbon atoms; and the other of the radicals R3 or R4 is selected from hydrogen; alkyl of 1 to 12 carbon atoms; cycloalkyl of 3 to 12 carbon atoms; phenyl, lower phenylalkyl where the alkyl radical contains from 1 to 6 carbon atoms, substituted phenyl and substituted lower phenylalkyl where said phenyl ring carries one or two substituents independently selected from the group consisting of hydroxy, lower alkyl, lower alkoxy and halogen; a terminally substituted alkyl group of 2 to 12 carbon atoms, with a substituted terminal carbon atom bearing 1 to 3 substituents independently selected from the group consisting of hydroxy, acyloxy of 2 to 12 carbon atoms, and alkoxy of 1 to 6 carbon atoms; and formula groups **(See formula)** where n is an integer from 1 to 4 and R8 and R9 are independently selected from hydrogen and alkyl groups of 1 to 4 carbon atoms and R10 is cycloalkyl of 3 to 8 carbon atoms; R7 is hydrogen, lower alkyl, aryl, or arylalkyl; and also with the condition that when Z is (see formula), then R4 cannot be hydrogen; whose procedure consists of hydrolyzing the corresponding compounds of formula: **(See formula)** where Z and R7 are those defined above, under acidic or basic conditions, thereby forming the corresponding compound of formula Ia. (Machine-translation by Google Translate, not legally binding)
机译:一种制备式为**(参见式)**的1-氨基(取代的)-3-(4'-或5'-噻唑(取代的-2-氧基)-2-丙醇衍生物的方法2是噻唑环上4或5位任意位置上的噻唑环上的取代基,选自下式的组:**(参见下式)**其中R3或R4之一独立地选自7至12个碳的烷基原子3至12个碳原子的环烷基; 2至12个碳原子的末端取代的烷基,其中取代的末端碳原子带有1至3个独立地选自羟基,2至12个碳原子的酰氧基和1至6个碳原子的烷氧基的取代基; (n为1至4的整数),R 8和R 9独立地选自氢和具有1至4个碳原子的烷基,并且R 10为具有3至8个碳的环烷基原子R3或R4中的另一个选自氢; 1至12个碳原子的烷基; 3至12个碳原子的环烷基;苯基,低级苯基烷基(其中烷基含有1至6个碳原子),取代的苯基和取代的低级苯基烷基(其中所述的苯环带有一个或两个独立地选自羟基,低级烷基,低级烷氧基和卤素的取代基);具有2至12个碳原子的末端取代的烷基,其中具有1至3个取代基的取代的末端碳原子独立地选自羟基,2至12个碳原子的酰氧基和1至6个碳原子的烷氧基。通式(**),其中n是1-4的整数,R8和R9独立地选自氢和1-4个碳原子的烷基,R10是3-8个碳原子的环烷基。 R7是氢,低级烷基,芳基或芳基烷基;并且当Z为(见公式)时,R4不能为氢;其程序包括在酸性或碱性条件下水解相应的式:**(参见式)**的化合物,其中Z和R 7为以上定义的那些,从而形成相应的式Ia的化合物。 (通过Google翻译进行机器翻译,没有法律约束力)

著录项

  • 公开/公告号ES446566A1

    专利类型

  • 公开/公告日1977-11-01

    原文格式PDF

  • 申请/专利权人 SYNTEX (U.S.A.) INC.;

    申请/专利号ES19760446566

  • 发明设计人

    申请日1976-03-31

  • 分类号C07D;A61K;

  • 国家 ES

  • 入库时间 2022-08-23 00:28:53

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