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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1809485Erstellt: 25. Oktober 2026

2-(3-Methoxy-allylidene)-malonic acid dimethyl ester → (S)-3-[2-tert-Butoxycarbonyl-2-(3-methoxycarbonyl-2-oxo-2H-pyridin-1-yl)-ethyl]-indole-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1809485

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-(3-Methoxy-allylidene)-malonic acid dimethyl esterHCID 597992—
Edukttert-butyl 3-[(2S)-2-amino-3-(tert-butoxy)-3-oxopropyl]-1H-indole-1-carboxylateHCID 7021141—
EduktSodium MethoxideHCID 10942334—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
Produkt(S)-3-[2-tert-Butoxycarbonyl-2-(3-methoxycarbonyl-2-oxo-2H-pyridin-1-yl)-ethyl]-indole-1-carboxylic acid tert-butyl esterHCID 5867495866,2%

Reaktionsschritte

To a solution of (S)-3-(2-Amino-2-tert-butoxycarbonyl-ethyl)-indole-1-carboxylic acid tert-butyl ester (2.5 g, 7 mmol) in methanol (15 ml) was added 2-(3-methoxy-allylidene)-malonic acid dimethyl ester (1.5 g, 7 mmol) and stirred overnight at room temperature. Sodium methoxide (78 mg, 1.4 mmol) was added and stirred for three hours at room temperature. The reaction mixture was diluted with water (50 ml) and extracted with ethylacetate (60 ml). The organic layer was washed with brine, dried (MgSO4), filtered and evaporated to afford the crude product, which was perified by flash chromatography (30-70% ethylacetate/petroleum ether) to afford the title compound as a white solid (2.3 g, 57%); 1H NMR (400 MHz, CDCl3) δ 1.43 (9H, s), 1.72 (9H, s), 3.50 (2H, m), 3.91 (3H, m), 5.68 (1H, br s), 6.08 (1H, t), 7.2-7.5 (5H, m), 8.15 (2H, m); M+H 497.5, M−H 495.5.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08362043B2
Quelldatensatzuspto-grants-2013_01
ORD IDord-38fcff9909d849b1905c205bec0fe92c
Quellennotizuspto-grants-2013_01