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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1181358Erstellt: 26. Oktober 2026

Ethanol → HCID 58980794, Verbindung

https://huagongshe.com/reaction/1181358

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
EduktMethyl 3-amino-5-(4-chlorophenyl)thiophene-2-carboxylateHCID 2777492—
EduktHCID 58980809HCID 58980809—
ProduktHCID 58980794HCID 5898079422%

Reaktionsbedingungen

Temperatur110 °C

Reaktionsschritte

Methyl 3-amino-5-(4-chlorophenyl)thiophene-2-carboxylate (0.1367 g, 0.5107 mmol) was taken up in dimethylformamdide dimethyl acetal (3 mL) and heated to 110° C. The reaction was stirred for 3 h and then concentrated. 4-[2-(3,3-Difluoropyrrolidin-1-yl)ethoxy]-3-methoxyaniline (0.1389 g, 0.5107 mmol) in absolute ethanol (3 mL) was added to the residue and concentrated. Fresh absolute ethanol (1 mL) was added and the reaction heated to reflux. The reaction was stirred for 18 h and then cooled to RT and the precipitate was collected to give 0.058 g (0.1120 mmol, 22%) of the product as a white solid. 1H NMR (D6-DMSO) δ 8.38 (s, 1H), 7.96 (s, 1H, 7.91 (d, 2H, J=8.4 Hz), 7.56 (d, 2H, J=8.4 Hz), 7.18 (s, 1H), 7.11 (d, 1H, J=8.5 Hz), 7.04 (d, 1H, J=8.6 Hz), 4.12 (t, 2H, J=5.5 Hz), 3.77 (s, 3H), 3.00 (t, 2H, J=13.6 Hz), 2.85 (t, 2H, J=5.5 Hz), 2.81 (t, 2H, J=7.0 Hz), 2.22 (m, 2H). LRMS M+H

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07285557B2
Quelldatensatzuspto-grants-2007_10
ORD IDord-74bdd90efa794466941a4ce6f3c5a473
Quellennotizuspto-grants-2007_10