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HRID 81227Erstellt: 26. Oktober 2026

3-Fluoro-2-pyridinecarboxaldehyde → HCID 178461203, Verbindung

https://huagongshe.com/reaction/81227

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-Fluoro-2-pyridinecarboxaldehydeHCID 11344017—
EduktHCID 178424953HCID 178424953—
EduktHCID 178461250HCID 178461250—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 178461203HCID 178461203—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

To a stirred solution of 6-chloro-4-(5-chloropyridin-3-yl)-3-[(trans-4-methylcyclohexyl)methyl]-3H-imidazo[4,5-c]pyridine (Preparative Example 3.1, Step 1) (1.2 g, 3.19 mmol) in THF (20 mL) was added 2,2,6,6-tetramethylpiperidinylmagnesium chloride lithium chloride complex (Aldrich, 1M in THF/toluene) (5.11 mL, 5.11 mmol) at −78° C., and the reaction was stirred at −78° C. for 2 hours under a nitrogen atmosphere. 3-fluoropicolinaldehyde (1.1 g, 9.59 mmol) dissolved in THF (4.0 mL) was added dropwise at −78° C., and the reaction was stirred for an additional 2 hours at −78° C. The reaction was quenched with aqueous saturated NH4Cl solution (50 mL) and extracted with ethyl acetate (2×40 mL). The combined organic extracts were washed with brine (20 mL), dried over anhydrous Na2SO4, filtered, and concentrated. Purification of the residue on a silica gel column (0 to 100% EtOAc/hexanes) afforded {6-chloro-4-(5-chloropyridin-3-yl)-3-[(trans-4-methylcyclohexyl)methyl]-3H-imidazo[4,5-c]pyridin-2-yl}(3-fluoropyridin-2-yl)methanol. MS APCl calcd. for C25H24Cl2FN5O [M+H]+ 500. found 500.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08846657B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-c4e04b20d00b456a88db4496f9bbdc08
Quellennotizuspto-grants-2014_09