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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1777034Erstellt: 26. Oktober 2026

3-Acetylpyridine → 3-morpholin-4-ylsulfonyl-N-[(E)-1-pyridin-3-ylethylideneamino]benzamide

https://huagongshe.com/reaction/1777034

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-AcetylpyridineHCID 9589—
Edukt3-(Morpholine-4-sulfonyl)benzohydrazideHCID 877246—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelMethanolHCID 887—
Produkt3-morpholin-4-ylsulfonyl-N-[(E)-1-pyridin-3-ylethylideneamino]benzamideHCID 4299114427,6%

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

3-(Morpholinosulfonyl)benzohydrazide (40 mg, 0.140 mmol) and 1-(pyridin-3-yl)ethanone (16.98 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 (15 mg). 1H NMR (400 MHz, CDCl3): δ 9.53 (bs, 1H), 8.87 (s, 1H), 8.59 (m, 1H), 8.39 (m, 1H), 8.17 (m, 1H), 7.98 (m, 1H), 7.89 (d, 1H, J=8.0 Hz), 7.67 (t, 1H, J=8.0 Hz), 7.32 (m, 1H), 3.70 (m, 4H), 3.00 (m, 4H), 2.39 (s, 3H). ESI-MS: 389.0 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09266838B2
Quelldatensatzuspto-grants-2016_02
ORD IDord-c1d4bc17c54c4421bd6d12c5796781d6
Quellennotizuspto-grants-2016_02