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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 216287Erstellt: 25. Oktober 2026

Diethylamine → methyl(2S)-3,3-dimethyl-2-{3-[(1-methyl-1H-benzimidazol-2-yl)methyl]-2-oxoimidazolidin-1-yl}butanoate

https://huagongshe.com/reaction/216287

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethylamineHCID 8021—
EduktBis(4-nitrophenyl) carbonateHCID 78756—
Eduktmethyl(2S)-2-[(2-{[(9H-fluoren-9-ylmethoxy)Carbonyl][(1-methyl-1H-benzimidazol-2-yl)methyl]amino}ethyl)amino]-3,3-dimethylbutanoateHCID 66891668—
LösungsmittelDimethylformamideHCID 6228—
Lösungsmittel1,1-DichloroethaneHCID 6365—
Produktmethyl(2S)-3,3-dimethyl-2-{3-[(1-methyl-1H-benzimidazol-2-yl)methyl]-2-oxoimidazolidin-1-yl}butanoateHCID 6689062965,2%

Reaktionsbedingungen

Temperatur25 °C

Reaktionsschritte

A solution of the product of Example 148D (0.19 g) in N,N-dimethylformamide (3.5 mL) was treated with diethylamine (0.35 mL), stirred at 25° C. for 1.5 hours and concentrated. A solution of the residue in dichloroethane (7 mL) was treated with bis-(p-nitrophenyl) carbonate (0.128 g, 1.2 equivalents), stirred at 60° C. for 16 hours and concentrated. The residue was chromatographed on silica gel, eluting with ethyl acetate:dichloromethane (3:2) to give 80 mg (64%) of the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08193227B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-b55997fdd53846e78ed6c4674a48a0e7
Quellennotizuspto-grants-2012_06