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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 555880Erstellt: 25. Oktober 2026

Benzimidazole → 1H-Benzo[D]imidazole-2-YL(4-(3-(tetrahydro-2H-thiopyran-4-YL)pyrazin-2-yloxy)phenyl)methanone

https://huagongshe.com/reaction/555880

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzimidazoleHCID 5798—
EduktBenzenesulfonic AcidHCID 7371—
EduktDiisopropylamineHCID 7912—
EduktPropane, 2,2',2''-[methylidynetris(oxy)]tris-HCID 78191—
EduktLithium diisopropylamideHCID 2724682—
EduktN-Methoxy-N-methyl-4-(3-(tetrahydro-2H-thiopyran-4-YL)pyrazin-2-yloxy)benzamideHCID 59351159—
LösungsmittelTolueneHCID 1140—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1H-Benzo[D]imidazole-2-YL(4-(3-(tetrahydro-2H-thiopyran-4-YL)pyrazin-2-yloxy)phenyl)methanoneHCID 59351128—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

A mixture of 1H-benzo[d]imidazole (0.039 g, 0.334 mmol), triisopropoxymethane (0.529 g, 2.78 mmol), benzenesulfonic acid (2.200 mg, 0.014 mmol) in toluene (5 mL) was heated at reflux for 3 h. The mixture was cooled, neutralized with diisopropylamine (0.1 ml), concentrated to dryness and diluted with 1 ml THF. The above solution was added to a stirred mixture of N-methoxy-N-methyl-4-(3-(tetrahydro-2H-thiopyran-4-yl)pyrazin-2-yloxy)benzamide (0.100 g, 0.278 mmol) in THF (3 mL). The resulting mixture was cooled to 0° C. and LDA (0.167 mL, 0.334 mmol) was added dropwise. The reaction mixture was stirred at RT overnight, quenched with saturated NH4Cl, extracted with EtOAc (3×), dried over MgSO4, concentrated and purified by ISCO (0-5% MeOH/DCM) to give the title compound as a white solid. MS (ESI, pos. ion) m/z: 416.1 (M+1). IC50 (uM) +++++.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08053438B2
Quelldatensatzuspto-grants-2011_11
ORD IDord-7f607c30c0094b30b3f5737be1cda2ec
Quellennotizuspto-grants-2011_11