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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 883688Erstellt: 26. Oktober 2026

Diisopropylcarbodiimide → methyl-2-[(3,5-dimethoxyphenyl)amino]-1-{3-[methyl(2-pyridin-2-ylethyl)amino]propyl}-1H-benzimidazole-5-carboxylate

https://huagongshe.com/reaction/883688

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylcarbodiimideHCID 12734—
Edukt3,5-Dimethoxyphenyl isothiocyanateHCID 145422—
EduktMethyl 3-amino-4-({3-[methyl(2-pyridin-2-ylethyl)amino]propyl}amino)benzoateHCID 69027376—
LösungsmittelTetrahydrofuranHCID 8028—
Produktmethyl-2-[(3,5-dimethoxyphenyl)amino]-1-{3-[methyl(2-pyridin-2-ylethyl)amino]propyl}-1H-benzimidazole-5-carboxylateHCID 6902764276%

Reaktionsschritte

3,5 dimethoxyphenylisothiocyanate (571 mg, 1 eq) and diisopropylcarbodiimide (1.35 ml, 4 eq) are added successively to a solution of methyl 3-amino-4-({3-[methyl(2-pyridin-2-ylethyl)amino]propyl}amino)benzoate (1.0 g, 1 eq) in tetrahydrofuran (10 ml). The mixture is heated under reflux for 18 hours then cooled down to ambient temperature and concentrated under reduced pressure at 40° C. The residue is taken up in ethyl acetate (100 ml) and water (40 ml). After decanting and extracting, the combined organic phases are washed with salt water, dried over Na2SO4 then evaporated under reduced pressure at 40° C. Purification of the residue by flash chromatography on silica gel (eluent: dichloromethane/methanol 99:1 to 98:2) produces the expected compound in the form of a beige foam (1.12 g; 76% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08236965B2
Quelldatensatzuspto-grants-2012_08
ORD IDord-e50e5f5eb4b64e4e9d1729119a561606
Quellennotizuspto-grants-2012_08