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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 705482Erstellt: 25. Oktober 2026

N,N'-Dimethylethylenediamine → N-(3-chloro-1-(pyridin-3-yl)-1H-pyrazol-4-yl)acetamide

https://huagongshe.com/reaction/705482

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN,N'-DimethylethylenediamineHCID 8070—
Edukt3-BromopyridineHCID 12286—
EduktPotassium Phosphate, TribasicHCID 62657—
Edukt3-IodopyridineHCID 70714—
EduktN-(3-chloro-1H-pyrazol-4-yl)acetamideHCID 178474372—
KatalysatorCopperHCID 23978—
ProduktN-(3-chloro-1-(pyridin-3-yl)-1H-pyrazol-4-yl)acetamideHCID 118023019—

Reaktionsschritte

In step c of Scheme 1, N-(3-chloro-1H-pyrazol-4-yl)acetamide (1b) is reacted with a halopyridine such as 3-bromopyridine or 3-iodopyridine in the presence of a copper salt (such as copper(I) chloride (CuCl), copper(II) chloride (CuCl2), or copper(I) iodide (CuI)), potassium phosphate (K3PO4), and N,N′-dimethylethane-1,2-diamine to yield N-(3-chloro-1-(pyridin-3-yl)-1H-pyrazol-4-yl)acetamide (1c). It has been discovered that when copper(I) iodide is used that the yield of the reaction is greatly affected by the quality of the copper(I) iodide. The process may be conducted in a polar solvent, such as, acetonitrile (MeCN), dioxane, or N,N-dimethylformamide at a temperature between about 50° C. and about 110° C. It was surprisingly discovered that the addition of water during the work-up of this step maximizes the yield. Further, this synthetic method is simpler and reduces the costs of starting materials over known heteroarylation methods.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09174962B2
Quelldatensatzuspto-grants-2015_11
ORD IDord-9a5e215d9d4740979c063d9f1c47c95b
Quellennotizuspto-grants-2015_11