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HRID 63593Erstellt: 24. Oktober 2026

Diisopropylethylamine → 2-Amino-5-chloro-4-(4-(5-methyl-1,2,4-oxadiazol-3-yl)methylpiperazin-1-yl)-3-nitropyridine

https://huagongshe.com/de/reaction/63593

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
Edukt2-Amino-4,5-dichloro-3-nitropyridineHCID 46867660—
Edukt1-[(5-Methyl-1,2,4-oxadiazol-3-yl)methyl]piperazine hydrochlorideHCID 75530688—
LösungsmittelIsopropanolHCID 3776—
Produkt2-Amino-5-chloro-4-(4-(5-methyl-1,2,4-oxadiazol-3-yl)methylpiperazin-1-yl)-3-nitropyridineHCID 7148147370,2%

Reaktionsbedingungen

Temperatur45 °C

Reaktionsschritte

1-[(5-Methyl-1,2,4-oxadiazol-3-yl)methyl]piperazine hydrochloride (217 mg, 0.99 mmol) and 2-amino-4,5-dichloro-3-nitropyridine (208 mg, 1.0 mmol) were stirred in 2-propanol (5 mL) and diisopropylethylamine (523 μL, 387 mg, 3.0 mmol) was added. The mixture was stirred and heated at 45° C. for 23 h. The reaction was cooled and the product filtered off and washed with 2-propanol. Drying in vacuum gave the product (246 mg, 69%). 1H-NMR (500 MHz, CDCl3), 2.63 (s, 3H, CH3), 2.77 (br m, 4H, piperazine C—H), 3.29 (m, 4H, piperazine C—H), 3.76 (s, 2H, CH2), 5.27 (s, 2H, NH2), 8.02 (s, 1H, pyridine 6-H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09447092B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-ca11d6524ce540f6b793af1492dd8c08
Quellennotizuspto-grants-2016_09