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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 12442Erstellt: 24. Oktober 2026

Benzo-1,3-dioxole-5-acetic acid → 3-((Benzo[d][1,3]dioxol-5-yl)methyl)-6-(thiophen-2-yl)-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazole

https://huagongshe.com/de/reaction/12442

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzo-1,3-dioxole-5-acetic acidHCID 76115—
Edukt2-Thiophenecarbonyl chlorideHCID 78928—
EduktSodium BicarbonateHCID 516892—
EduktThiocarbohydrazideHCID 2724189—
LösungsmittelChlorideHCID 312—
LösungsmittelDichloromethane methanolHCID 21226129—
Produkt3-((Benzo[d][1,3]dioxol-5-yl)methyl)-6-(thiophen-2-yl)-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazoleHCID 16736061—

Reaktionsbedingungen

Temperatur170 °C

Reaktionsschritte

As shown in FIG. 2, 2-(benzo[d][1,3]dioxol-5-yl)acetic acid (1 mmol) and thiocarbonohydrazide (1.5 mmol) were heated at 170° C. for 15 min. The mixture was cooled and taken up in 5% MeOH/CH2Cl2 and saturated NaHCO3. The organics were washed with water, saturated NaCl, dried over Na2SO4, and concentrated in vacuo. The resulting 5-((benzo[d][1,3]dioxol-5-yl)methyl)-4H-4-amino-3-mercapto-1,2,4-triazole (compound 1001) was used as is in the next reaction. Accordingly, a mixture of compound 1001 and thiopene-2-carbonyl chloride (0.176 g, 1.2 mmol) suspended in excess phoshoryl chloride (˜10 mL) was refluxed 5 hours. The excess phoshoryl chloride was removed under reduced pressure and the subsequent residue was mixed with crushed ice. The solids were filtered, washed with water, and dried in vaciio. Purification by reversed-phase HPLC produced pure 3-((benzo[d][1,3]dioxol-5-yl)methyl)-6-(thiophen-2-yl)-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazole (compound 2).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07728017B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-ecce3c714f654f259f67249d6ff0a797
Quellennotizuspto-grants-2010_06