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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 877619Erstellt: 25. Oktober 2026

5'-Chloro-2'-hydroxypropiophenone → N-[(E)-1-(5-chloro-2-hydroxyphenyl)propylideneamino]-3-morpholin-4-ylsulfonylbenzamide

https://huagongshe.com/reaction/877619

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt5'-Chloro-2'-hydroxypropiophenoneHCID 292114—
Edukt3-(Morpholine-4-sulfonyl)benzohydrazideHCID 877246—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelMethanolHCID 887—
ProduktN-[(E)-1-(5-chloro-2-hydroxyphenyl)propylideneamino]-3-morpholin-4-ylsulfonylbenzamideHCID 13627661631,6%

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

3-(Morpholinosulfonyl)benzohydrazide (40 mg, 0.140 mmol) and 1-(5-chloro-2-hydroxyphenyl)propan-1-one (25.9 mg, 0.140 mmol) were dissolved in methanol (4 mL) in the presence of acetic acid as a catalyst, and the reaction mixture was heated via microwave irradiation to 120° C. for 30 min. The reaction was monitored by TLC. Upon completion of the reaction and following cooling, the solvent was removed by vacuum, and the resulting crude material was purified by flash column chromatography (2% CH3OH/CH2Cl2) affording the title compound as a solid (20 mg). 1H NMR (400 MHz, acetone-d6): δ 8.26 (m, 2H), 8.00 (d, 1H, J=7.6 Hz), 7.84 (t, 1H, J=8.0 Hz), 7.64 (d, 1H, J=2.4 Hz), 7.33 (m, 1H), 6.98 (d, 1H, J=9.2 Hz), 3.69 (m, 4H), 3.10 (q, 2H, J=7.6 Hz), 2.99 (m, 4H), 1.26 (t, 3H, J=7.6 Hz). ESI-MS: 452.1 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08987335B2
Quelldatensatzuspto-grants-2015_03
ORD IDord-48e542c34ed448839a3842b27da61f5e
Quellennotizuspto-grants-2015_03