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A process for the preparation of an aspartyl dipeptide amide L - A - D - amino acid.

机译:一种天冬氨酰二肽酰胺L-A-D-氨基酸的制备方法。

摘要

Process for the preparation of an aspartyl dipeptide amide L - A - D - amino acid.Consists in: a) reacting carboxianhidrido tio n - L - aspartyl of formula (ii) with an amide of a d-amino acid of formula (iii) in the presence of Aqueous Solvent at basic pH, and then to produce the destiocarboxilacion acidify the resulting Intermediate; and (b) The dipeptid crystallize Or L - aspartate - D - amino acid of formula (i) with an Aromatic sulfonic acid of formula (iv)Where R is Hydrogen or hydroxyl; and is represented by groups of formula (V), where r, r, R and R is alkyl, C 1 to 4 and the remaining are Hydrogen or alkyl C 1 to 4; X is o, S, so, SO2 and other; M is 0, 1 2, 3 or 4; n, P and q are 0, 1, 2 or 3, with the condition that n is not greater than 3 b p; R is Chlorine and Hydrogen or Methyl; R is Hydrogen or Methyl.Have applications for its sweetening Properties.
机译:一种天冬氨酰二肽酰胺L-A-D-氨基酸的制备方法,包括:a)使式(ii)的羧甲基-L-天冬氨酰与式(iii)的d-氨基酸的酰胺反应在碱性pH的水溶液中存在,然后产生去羧羧甲酰化酸化所得的中间体; (b)用式(iv)的芳族磺酸使式(i)的二肽或L-天冬氨酸-D-氨基酸结晶,其中R是氢或羟基;并且由式(V)的基团表示,其中r,r,R 1和R 2为烷基,C 1至4,其余为氢或烷基C 1至4; X是o,S,所以是SO2等; M为0、1、2、3或4; n,P和q为0、1、2或3,条件是n不大于3 b p; R是氯和氢或甲基; R是氢或甲基。具有甜味特性。

著录项

  • 公开/公告号ES8406064A1

    专利类型

  • 公开/公告日1984-10-16

    原文格式PDF

  • 申请/专利权人 PFIZER INC.;

    申请/专利号ES19830521765

  • 发明设计人

    申请日1983-04-22

  • 分类号C07C103/52;A23L1/236;

  • 国家 ES

  • 入库时间 2022-08-22 09:05:36

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