Invention Grant
US08278478B2 Process for the synthesis of hydrochloride salt of N-fatty acylsubstituted amino acid ethyl esters 有权
合成N-脂肪酰基取代氨基酸乙酯盐酸盐的方法

  • Patent Title: Process for the synthesis of hydrochloride salt of N-fatty acylsubstituted amino acid ethyl esters
  • Patent Title (中): 合成N-脂肪酰基取代氨基酸乙酯盐酸盐的方法
  • Application No.: US12888583
    Application Date: 2010-09-23
  • Publication No.: US08278478B2
    Publication Date: 2012-10-02
  • Inventor: Vishwas Sadhu Ghare
  • Applicant: Vishwas Sadhu Ghare
  • Agency: Lucas & Mercanti, LLP
  • Agent Robert P. Michal
  • Main IPC: C07C229/00
  • IPC: C07C229/00
Process for the synthesis of hydrochloride salt of N-fatty acylsubstituted amino acid ethyl esters
Abstract:
The present invention relates to a process for preparing hydrochloride salt of N-fatty acyl substituted amino acid ethyl ester. Said process includes the steps of: dissolving L-arginine ethyl ester dihydrochloride in distilled water with continuous agitation for a period of about 10 to about 20 minutes to obtain a clear solution; lowering the temperature of the clear solution to about 5° C. to about 10° C. to obtain a cooled solution; adjusting the pH of the cooled solution in the range of about 7 to about 8 by adding sodium hydroxide solution; adding at least one organic solvent to the clear solution with continuous agitation to obtain an intermediate mixture; condensing the intermediate mixture by simultaneously adding an acid halide and 20% sodium hydroxide solution at a temperature of about 7° C. to about 9° C. and at a pH in the range of about 7.2 to about 7.5 for about 2 hours to obtain a mixture; raising the temperature of the mixture to about 18 to about 20° C. followed by addition of sodium hydroxide to adjust the pH of the mixture to about 7.3; warming the mixture at a temperature of about 25 to about 30° C. to obtain a resultant mixture containing organic phase and aqueous phase; separating the organic phase and aqueous phase of the resultant mixture by settling the mixture; and distilling the organic phase under vacuum at a temperature of about 70° C. to about 75° C. to obtain a hydrochloride salt of ethyl lauroyl arginate.
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