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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 15028Erstellt: 23. Oktober 2026

4-(Morpholin-4-yl)benzoic acid → 6-(4-Morpholinophenyl)-3-(3,4,5-trimethoxyphenyl)-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazole

https://huagongshe.com/de/reaction/15028

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-(Morpholin-4-yl)benzoic acidHCID 345278—
EduktHCID 178488244HCID 178488244—
LösungsmittelPhosphorus oxychlorideHCID 24813—
Produkt6-(4-Morpholinophenyl)-3-(3,4,5-trimethoxyphenyl)-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazoleHCID 2495522824,4%

Reaktionsschritte

A mixture of 4-morpholinobenzoic acid (86 mg, 0.42 mmol) and 4-amino-3-mercapto-5-(3,4,5-trimethoxyphenyl)-4H-1,2,4-triazole (102 mg, 0.36 mmol) was refluxed in POCl3 (5 mL) for 2 h. The reaction mixture was cooled to room temperature and excess POCl3 was removed under vacuum. The residue was dissolved in ethyl acetate and washed with saturated NaHCO3. The organic layer was dried over anhydrous Na2SO4, filtered and concentrated. The crude product was purified by chromatography (80% ethyl acetate/hexane; 1 mL methanol/100 mL of solvent) to give the title compound as a yellow solid (40 mg, 0.088 mmol, 24%). 1H NMR (CDCl3): 7.78 (m, 2H), 7.73 (s, 2H), 6.98 (m, 2H), 4.00 (s, 6H), 3.94 (s, 3H), 3.89 (m, 4H), 3.41 (m, 4H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07732468B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-1a99ddf1b32949a193135c68e1c70694
Quellennotizuspto-grants-2010_06