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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 852902Erstellt: 25. Oktober 2026

Phenylsilane → Methyl 4-([2,3']bipyridinyl-6-ylaminomethyl)-benzoate

https://huagongshe.com/reaction/852902

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhenylsilaneHCID 12752—
EduktMethyl 4-FormylbenzoateHCID 15294—
Edukt[2,3'-Bipyridin]-6-amineHCID 11586359—
KatalysatorDibutyltin dichlorideHCID 12688—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktMethyl 4-([2,3']bipyridinyl-6-ylaminomethyl)-benzoateHCID 5893061098,3%

Reaktionsschritte

To a stirred suspension of a mixture of 11 (3.00 g, 17.52 mmol), methyl 4-formylbenzoate (4.62 g, 28.11 mmol, 1.5-2.0 equiv.) and dibutyl tin dichloride 160 mg, 0.53 mmol) in anhydrous THF (15 mL) at room temperature was added phenylsilane (2.34 mL, 19.28 mmol) in three portions over two days. After stirring for 2 to 7 days the reaction mixture was filtered, filtrate was concentrated and purified by flash chromatography on silica gel (MeOH/CH2Cl2, 2/98→10/90) to afford the title compound 12 (5.50 g, 17.22 mmol, 98% yield) as a pale yellow solid. 1H NMR (400 MHz, DMSO-d6) δ (ppm): 9.11 (dd, J=2.3, 0.7 Hz, 1H), 8.55 (dd, J=4.7, 1.8 Hz, 1H), 8.29-8.24 (m, 1H), 7.93 (d, J=8.4 Hz, 2H), 7.57-7.40 (m, 5H), 7.18 (d, J=7.2 Hz, 1H), 6.59 (d, J=8.2 Hz 1H), 4.69 (d, J=6.1 Hz, 2H), 3.85 (s, 3H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07253204B2
Quelldatensatzuspto-grants-2007_08
ORD IDord-cdbb4155d2954433adc05ef0eed4ec93
Quellennotizuspto-grants-2007_08