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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 278034Erstellt: 24. Oktober 2026

Diisopropylamine → HCID 178509145, Verbindung

https://huagongshe.com/de/reaction/278034

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylamineHCID 7912—
EduktO-[(Ethoxycarbonyl)cyanomethylenamino]-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733286—
Edukt5-(1-Amino-3-phenylpropyl)-[1,3,4]oxadiazol-2-ylamineHCID 22626939—
EduktHCID 178524160HCID 178524160—
LösungsmittelDimethylformamideHCID 6228—
ProduktHCID 178509145HCID 178509145—

Reaktionsschritte

0.18 g of 5-(1-amino-3-phenylpropyl)-[1,3,4]oxadiazol-2-ylamine was dissolved in 10 ml of dry dimethylformamide at RT, treated with 200 mg of 2-pyridin-4-yl-1H-benzimidazole-5-carboxylic acid, 270 mg of TOTU, and 0.12 ml of diisopropylamine, and stirred at RT for 4 h. The reaction mixture was concentrated, and the residue was taken up in ethyl acetate and washed successively with water, saturated sodium hydrogencarbonate solution, water, and saturated sodium chloride solution. The organic phase was dried over magnesium sulfate, filtered, and concentrated. The residue was stirred with methyl tert-butyl ether, filtered off, and dried under high vacuum. 2-Pyridin4-yl-1H-benzimidazole-5-carboxylic acid [1-(5-amino-[1,3,4]oxadiazol-2-yl)-3-phenylpropyl]amide, which melts at 160° C. with decomposition, is obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06358978B1
Quelldatensatzuspto-grants-2002_03
ORD IDord-f71fbc6784cd47cc9dde6ac5c08115e2
Quellennotizuspto-grants-2002_03