All articles of this category A short and efficient synthesis of the novel cholinergic channel activator ABT 418, ( S )-3-methyl-5-(1-methyl-2-pyrrolidinyl)isoxazole, has been developed. The four-step route from L-proline afforded the target compound in ca. 35% overall yield in very high chemical and enantiomeric purity. This route has afforded multigram quantities of the clinical candidate and should be amenable to kilogram-scale reactions. ABT 418 was synthesized in four steps (35% yield) from (L)-proline
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Elliott et al. (1995) studied this question.