Development of a Convergent and Scalable Synthetic Route to Long-Acting RSV Inhibitor JNJ-7950

可扩展性 计算机科学 化学 组合化学 数据库
作者
Kiran Matcha,William Maton,Peter Reniers,Robert Geertman,Bart Bueken,Philip J. Pye,Stijn Wuyts,Ed Cleator
出处
期刊:Organic Process Research & Development [American Chemical Society]
卷期号:29 (4): 1036-1047 被引量:2
标识
DOI:10.1021/acs.oprd.4c00437
摘要

JNJ-7950 is a potent small-molecule respiratory syncytial virus (RSV) inhibitor with a long-acting profile in preclinical species. The design and development of a convergent synthetic route accelerated the discovery and development of JNJ-7950. First, the new synthetic route supported the lead candidate (JNJ-7950) selection process and later was adapted to provide a large-scale clinical batch. A shorter and cost-effective synthetic route to the key spiro-azetidine moiety exploited an intramolecular copper-catalyzed C–N coupling. The development of an efficient and sustainable process for telescoping three steps in a single solvent provided the benzimidazole moiety with an 85% overall yield. The spiro-azetidine and the benzimidazole moieties were coupled to provide JNJ-7950 in 48% overall yield with excellent purity over the six longest linear steps. Two GMP batches (6 and 12 kg) of JNJ-7950 were manufactured in parenteral grade quality to support long-acting injectable formulation development and early clinical need.
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