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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2120239Erstellt: 24. Oktober 2026

Piperidine → HCID 54352759, Verbindung

https://huagongshe.com/de/reaction/2120239

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPiperidineHCID 8082—
Edukt4-(2-Hydroxyethyl)indolin-2-oneHCID 10943004—
Edukt4-Methoxy-3-(thiophen-2-yl)benzaldehydeHCID 21981024—
LösungsmittelEthanolHCID 702—
ProduktHCID 54352759HCID 5435275947%

Reaktionsschritte

A mixture of 4-(2-hydroxy-ethyl)-1,3-dihydro-indol-2-one (1.6 g, 9.2 mmol), 4-methoxy-3-thiophen-2-yl-benzaldehyde (2 g, 9.2 mmol) and piperidine (4.5 mL, 85 mmol) in ethanol (46 mL) was heated to reflux for overnight. The reaction mixture was concentrated and the residue was chromatographed on a column of silica gel to give 1.63 g (47%) of 4-(2-hydroxy-ethyl)-3-(4-methoxy-3-thiophen-2-yl-benzylidene)-1,3-dihydro-indol-2-one as a yellow orange solid. 1HNMR (300 MHz, DMSO-d6) δ 10.53 (s, br, 1H, NH), 8.73 (d, J=2.1 Hz, 1H), 8.10 (dd, J=2.2 & 9.1 Hz, 1H), 7.74 (s, 1H, H-vinyl), 7.56-7.65 (m, 2H), 7.07-7.22 (m, 3H), 6.81 (d, J=7.5 Hz, 1H), 6.68 (dd, J=0.6, 7.5 Hz, 1H), 4.87 (t, J=4.5 Hz, 1H, OH), 3.97 (s, 3H, OCH3), 3.68-3.75 (m, 2H, CH2CH2OH), 3.09 (t, J=4.5 Hz, 2H, CH2CH2OH).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06689806B1
Quelldatensatzuspto-grants-2004_02
ORD IDord-026f27878bb8434eb2bd152067b6cb4c
Quellennotizuspto-grants-2004_02