The invention provides non-oxidative methods for the large scale manufacture of pyridoxamine (I) (4-aminomethyl-3-hydroxy-5-hydroxymethyl-2-methylpyridine):
(I), and salts thereof. The invention also provides intermediate compounds for the synthesis of pyridoxamine, as well as compositions and methods for the treatment and/or prevention of conditions associated with the formation of post-Amadori advanced glycation end-products.
本发明提供了用于大规模制造
吡哆醇胺(I)(4-
氨甲基-3-羟基-
5-羟甲基-2-
甲基吡啶)及其盐的非氧化方法。本发明还提供了用于合成
吡哆醇胺的中间化合物,以及用于治疗和/或预防与后-Amadori高级糖基化终产物形成相关疾病的组合物和方法。