Preparation method of salazosulfapyridine
The invention provides a preparation method of salazosulfapyridine. The preparation method comprises the following steps: S1, carrying out a cyclic condensation reaction on sulfaguanidine serving as astarting raw material and a C3 active compound to obtain sulfadiazine; S2, dissolving the sulfadiazi...
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Format: | Patent |
Sprache: | chi ; eng |
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Zusammenfassung: | The invention provides a preparation method of salazosulfapyridine. The preparation method comprises the following steps: S1, carrying out a cyclic condensation reaction on sulfaguanidine serving as astarting raw material and a C3 active compound to obtain sulfadiazine; S2, dissolving the sulfadiazine obtained in the step S1 in an aqueous solution containing sodium nitrite for a diazotization reaction so as to further obtain a diazonium salt; and S3, transferring the diazonium salt obtained in the step S2 into an aqueous sodium hydroxide solution, and carrying out a coupling reaction with salicylic acid to finally obtain salazosulfapyridine. Aiming at the defects in the prior art, the invention provides the preparation method of salazosulfapyridine; and according to the preparation method, raw materials are easy to obtain, and the purity and yield of the obtained purified product are high.
本发明提供了一种柳氮磺吡啶的制备方法,包括以下步骤:S1:以磺胺脒为起始原料,与三碳活性化合物进行环状缩合反应获取磺胺嘧啶;S2:将步骤S1中的磺胺嘧啶溶解在含有亚硝酸钠的水溶液中进行重氮化反应,进一步获取重氮盐;S3:将步骤S2中获取的重氮 |
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