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双膦/镍催化酚与氯吡啶和相关亲电试剂的 C-O 交叉偶联。

Bisphosphine/Nickel-Catalyzed C-O Cross-Coupling of Phenols with Chloropyridine and Related Electrophiles.

机构信息

Department of Chemistry, Dalhousie University, 6274 Coburg Road, P.O. 15000, Halifax, Nova Scotia B3H 4R2, Canada.

出版信息

Org Lett. 2022 Dec 16;24(49):8986-8989. doi: 10.1021/acs.orglett.2c03587. Epub 2022 Dec 1.

Abstract

Notwithstanding recent developments in nickel-catalyzed C-O cross-coupling chemistry, such transformations of substituted phenols and (hetero)aryl chlorides with a useful reaction scope have yet to be reported. In this work, we disclose the results of catalyst screening that allowed the identification of PhPAd-DalPhos/NiCOD as an effective catalyst system under thermal conditions for the O-arylation of substituted phenols with chloropyridine-type electrophiles, leading to pyridyl--aryl frameworks that are found in active pharmaceutical ingredients.

摘要

尽管镍催化的 C-O 交叉偶联化学在最近取得了进展,但具有有用反应范围的取代苯酚和(杂)芳基氯化物的此类转化尚未见报道。在这项工作中,我们披露了催化剂筛选的结果,该筛选允许鉴定 PhPAd-DalPhos/NiCOD 作为在热条件下用于取代苯酚与氯代吡啶型亲电试剂的 O-芳基化的有效催化剂体系,得到了在活性药物成分中发现的吡啶基-芳基骨架。

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