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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2099830Erstellt: 27. Oktober 2026

N-Methyl dicyclohexylamine → 4-tert-Butyl 1-methyl 2-((7-methyl-2-((2-(trimethylsilyl)ethoxy)methyl)-2H-indazol-5-yl)methyl)succinate

https://huagongshe.com/reaction/2099830

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-Methyl dicyclohexylamineHCID 24210—
Edukt2-Chloromethyl 2-(trimethylsilyl)ethyl etherHCID 2724271—
Edukt4-Tert-Butyl 1-methyl 2-((7-methyl-1H-indazol-5-yl)methyl)succinateHCID 57794720—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-tert-Butyl 1-methyl 2-((7-methyl-2-((2-(trimethylsilyl)ethoxy)methyl)-2H-indazol-5-yl)methyl)succinateHCID 69072989—

Reaktionsschritte

To a solution of 4-tert-butyl 1-methyl 2-((7-methyl-1H-indazol-5-yl)methyl)succinate (0.6053 g, 1.82 mmol) and N-cyclohexyl-N-methylcyclohexanamine (0.4686 mL, 2.19 mmol) in tetrahydrofuran (10 mL) was added trimethylsilylethoxymethyl chloride (0.3859 mL, 2.19 mmol) at room temperature under nitrogen. The reaction was stirred overnight and the solvent was removed in vacuo. The crude product was taken up in ethyl acetate (10 mL) and washed with water (3×5 mL). The ethyl acetate layer was dried, filtered and concentrated. The final product was obtained by flash chromatography, eluting with 0% to 20% ethyl acetate/hexane. (0.5873 g, 70%) HPLC tR=1.89 min, MS(ESI)[M+H]+=462.94.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07569578B2
Quelldatensatzuspto-grants-2009_08
ORD IDord-0ef70621c5d8428ba9a0501e688a9681
Quellennotizuspto-grants-2009_08