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(S)-萘普生-苯并三唑的合成及其作为手性衍生试剂用于微波辅助合成和非对映异构体的间接高效液相色谱分离。

Synthesis of (S)-naproxen-benzotriazole and its application as chiral derivatizing reagent for microwave-assisted synthesis and indirect high performance liquid chromatographic separation of diastereomers of penicillamine, cysteine and homocysteine.

机构信息

Department of Chemistry, Indian Institute of Technology Roorkee, Roorkee-247667, India.

出版信息

J Chromatogr A. 2011 Jun 10;1218(23):3648-53. doi: 10.1016/j.chroma.2011.04.016. Epub 2011 Apr 14.

DOI:10.1016/j.chroma.2011.04.016
PMID:21530971
Abstract

(S)-Naproxen-benzotriazole was synthesized by the reaction of (S)-naproxen with 1H-benzotriazole using coupling reagent dicyclohexyl carbodiimide and 4-dimethylamino pyridine (DCC/DMAP). It was used as chiral derivatizing reagent for microwave irradiated synthesis of diastereomers of penicillamine, cysteine and homocysteine. The diastereomers were separated by reversed phase high performance liquid chromatography using gradient elution of triethylammonium phosphate (pH 3.5)-acetonitrile (30-65% within 30 min). The method was validated for accuracy, precision, and limit of detection.

摘要

(S)-萘普生-苯并三唑通过(S)-萘普生与 1H-苯并三唑在偶联试剂二环己基碳二亚胺和 4-二甲氨基吡啶(DCC/DMAP)的作用下合成。它被用作手性衍生试剂,用于微波照射下合成青霉素胺、半胱氨酸和高半胱氨酸的非对映异构体。非对映异构体通过反相高效液相色谱法,使用三乙铵磷酸盐(pH 3.5)-乙腈(在 30 分钟内 30-65%)梯度洗脱进行分离。该方法经过了准确性、精密度和检测限的验证。

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