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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 81283Erstellt: 24. Oktober 2026

Cesium carbonate → HCID 178461220, Verbindung

https://huagongshe.com/de/reaction/81283

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCesium carbonateHCID 10796—
EduktCyclobutylcarbinolHCID 78130—
EduktBinap, (A+-)-HCID 634876—
EduktHCID 178461219HCID 178461219—
KatalysatorBis(dibenzylideneacetone)palladiumHCID 9811564—
LösungsmittelDimethyl SulfoxideHCID 679—
ProduktHCID 178461220HCID 178461220—

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

To a solution of 4,6-dichloro-3-[(trans-4-methylcyclohexyl)methyl]-2-[(3R)-3-phenylmorpholin-4-yl]-3H-imidazo[4,5-c]pyridine (Example 2.1, Step 2; 400 mg, 0.87 mmol) in DMSO (5 mL) was added cyclobutylmethanol (337 mg, 3.92 mmol), Cs2CO3 (848 mg, 2.61 mmol) and BINAP (108 mg, 0.17 mmol). The reaction mixture was deoxygenated by purging with nitrogen for 10 minutes and then Pd2dba3 (159 mg, 0.17 mmol) was added. The reaction was again deoxygenated for 5 minutes by purging with nitrogen. The reaction flask was sealed, and the mixture was heated at 100° C. for 16 h. The reaction mixture was then cooled, diluted with water (30 ml) and EtOAc (60 mL), and the organic layer was separated. The organic layer was washed with water (2×10 mL), followed by saturated brine (2×30 mL). The organic layer was dried over anhydrous Na2SO4, filtered, and concentrated. The residue was purified on a silica gel column (30% EtOAc/petroleum ether) to yield 6-chloro-4-(cyclobutylmethoxy)-3-[(trans-4-methylcyclohexyl)methyl]-2-[(3R)-3-phenylmorpholin-4-yl]-3H-imidazo[4,5-c]pyridine. MS ES/APCl calc'd. for C29H37ClN4O2 [M+H]+ 509. found 509.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08846657B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-4080d3e218c94089919b724dd34a35eb
Quellennotizuspto-grants-2014_09