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HRID 220168Erstellt: 24. Oktober 2026

Diethyl Malonate → Diethyl 2-(5-bromopyridin-2-yl)malonate

https://huagongshe.com/de/reaction/220168

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl MalonateHCID 7761—
Edukt5-Bromo-2-iodopyridineHCID 593690—
Edukt2-(5-Bromo-pyridin-2-yl)-5-chloro-pentanoic acidHCID 59238266—
KatalysatorCopperHCID 23978—
ProduktDiethyl 2-(5-bromopyridin-2-yl)malonateHCID 59238270—

Reaktionsschritte

Key building block 2-(5-bromo-pyridin-2-yl)-5-chloro-pentanoic acid (XII) can be prepared according to Scheme 8. Starting with commercially available 5-bromo-2-iodo-pyridine (XXXV), copper-catalyzed reaction with malonic acid diethyl ester furnishes 2-(5-bromo-pyridin-2-yl)-malonic acid diethyl ester (XXXVI). Hydrolysis and decarboxylation under basic conditions gives (5-bromo-pyridin-2-yl)-acetic acid (XXXVII), which subsequently can undergo nucleophilic acyl substitution with thionyl chloride in methanol to provide (5-bromo-pyridin-2-yl)-acetic acid methyl ester (XXXVIII). Deprotonation of XXXVIII with strong base followed by alkylation with 1-bromo-3-chloropropane gives 2-(5-bromo-pyridin-2-yl)-5-chloro-pentanoic acid methyl ester (XXXIX), which can then be hydrolyzed under aqueous basic conditions to furnish key building block 2-(5-bromo-pyridin-2-yl)-5-chloro-pentanoic acid (XII).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08202866B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-d92c2f563d9b4e8c9c4fda92d65f3291
Quellennotizuspto-grants-2012_06