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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 2-(3-Methoxy-allylidene)-malonic acid dimethyl ester | HCID 597992 | — |
| Edukt | tert-butyl 3-[(2S)-2-amino-3-(tert-butoxy)-3-oxopropyl]-1H-indole-1-carboxylate | HCID 7021141 | — |
| Edukt | Sodium Methoxide | HCID 10942334 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | (S)-3-[2-tert-Butoxycarbonyl-2-(3-methoxycarbonyl-2-oxo-2H-pyridin-1-yl)-ethyl]-indole-1-carboxylic acid tert-butyl ester | HCID 58674958 | 66,2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08362043B2 |
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| Quelldatensatz | uspto-grants-2013_01 |
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| ORD ID | ord-38fcff9909d849b1905c205bec0fe92c |
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| Quellennotiz | uspto-grants-2013_01 |
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