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Synthetic method for anti-HIV active sulfonic acid based bagasse xylan p-ferrocene benzoate

A technology of benzoate and xylan, which is applied in the direction of antiviral agents, can solve the problems of limited anti-HIV activity, and achieve the effect of stable product quality and high utilization rate of raw materials

Inactive Publication Date: 2018-02-23
GUILIN UNIVERSITY OF TECHNOLOGY
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0003] Studies have shown that sulfoxylan has anti-HIV activity, but the anti-HIV activity produced by a single active group in the monoesterified derivative is limited. If further modification on the basis of the monoesterified derivative introduces other anti-biological active groups group, will significantly improve the anti-HIV activity of xylan esterified derivatives

Method used

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  • Synthetic method for anti-HIV active sulfonic acid based bagasse xylan p-ferrocene benzoate
  • Synthetic method for anti-HIV active sulfonic acid based bagasse xylan p-ferrocene benzoate
  • Synthetic method for anti-HIV active sulfonic acid based bagasse xylan p-ferrocene benzoate

Examples

Experimental program
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Embodiment

[0046] (1) Drying 10 g of bagasse xylan in a vacuum constant temperature drying oven at 60°C for 24 hours to constant weight to obtain dry bagasse xylan.

[0047] (2) 8g solid NaHSO 3 Add 30mL of distilled water into a 250mL four-necked flask in turn, stir and dissolve at room temperature to obtain a mass fraction of 21% NaHSO 3 solution.

[0048] (3) heating the NaHSO with a mass fraction of 21% obtained in step (2) under stirring 3 The solution was brought to 85°C, and 20% NaNO was added dropwise. 2 7 mL of the solution was added dropwise under control for 20 minutes, and the reaction was continued to stir for 15 minutes to obtain an esterification agent sodium sulfamate solution.

[0049] (4) Weigh 3 g of dry-based bagasse xylan obtained in step (1) and add it to the reaction system obtained in step (3), then add 0.03 g of catalyst 12-tungstophosphoric acid to it, control the reaction temperature to be 55°C, and add mass fraction It was 2 mL of 5% sodium hydroxide solut...

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Abstract

The invention discloses a preparation method for anti-HIV active sulfonic acid based bagasse xylan p-ferrocene benzoate. The preparation method comprises the following steps: with bagasse xylan as a raw material, sodium trisulphamidate as an esterifying agent of a reaction in a first step, and p-toluene sulphonic acid as a catalyst, carrying out an esterification reaction and hydrochloric acidizing treatment in an aqueous phase so as to obtain sulfonic acid based bagasse xylan, and determining the substitution degree of sulfation; and on the basis of synthesizing the sulfonic acid based bagasse xylan, and with p-ferrocene based benzoic acid as the carboxylating agent in a second step and phosphomolybdic acid as a catalyst, and carrying out an esterification reaction with the sulfonic acidbased bagasse xylan in a chloroform solvent so as to synthesize the sulfonic acid based bagasse xylan p-ferrocene benzoate. The preparation method has the following advantages: the sulfonic acid basedbagasse xylan p-ferrocene benzoate obtained by using the method provided by the invention has the biological activity of bagasse xylan sulfate; meanwhile, the anti-biological activity of p-ferrocenebenzoic acid is introduced; characteristics like high raw material utilization rate and stable product quality are obtained; and important application values in fields like biology, medicine and functional materials are realized.

Description

technical field [0001] The invention belongs to the technical field of fine chemicals, and in particular relates to a method for synthesizing anti-HIV active sulfonated bagasse xylan p-ferrocene benzoate. Background technique [0002] Converting a large amount of biomass resources in agriculture into biomass-based energy and functional materials has become an important research topic and social development trend that researchers at home and abroad pay attention to. In order to more effectively utilize agricultural and forestry biomass resources and promote the high-value conversion of hemicelluloses such as xylan, it is of great significance to chemically modify natural polysaccharides such as xylan. [0003] Studies have shown that sulfoxylan has anti-HIV activity, but the anti-HIV activity produced by a single active group in the monoesterified derivative is limited. If the monoesterified derivative is further modified to introduce other anti-biological active groups grou...

Claims

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Application Information

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IPC IPC(8): C08B37/14A61P31/18
CPCC08B37/0057
Inventor 李和平钱敬侠张淑芬孙彦苏念英黄红霞杨世军杨莹莹郑光绿
Owner GUILIN UNIVERSITY OF TECHNOLOGY
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