Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Diethyl Malonate | HCID 7761 | — |
| Edukt | 5-Bromo-2-iodopyridine | HCID 593690 | — |
| Edukt | 2-(5-Bromo-pyridin-2-yl)-5-chloro-pentanoic acid | HCID 59238266 | — |
| Katalysator | Copper | HCID 23978 | — |
| Produkt | Diethyl 2-(5-bromopyridin-2-yl)malonate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08202866B2 |
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| Quelldatensatz | uspto-grants-2012_06 |
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| ORD ID | ord-d92c2f563d9b4e8c9c4fda92d65f3291 |
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| Quellennotiz | uspto-grants-2012_06 |
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