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HRID 626665Erstellt: 25. Oktober 2026

Ammonia → 2-(2,6-Dichlorophenyl)-2h-pyrazolo[4,3-c]pyridin-4-amine

https://huagongshe.com/reaction/626665

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmoniaHCID 222—
EduktN-[2-(2,6-dichlorophenyl)-2H-pyrazolo[4,3-c]pyridine-4-yl]-N'-methylpyrimidine-4,6-diamineHCID 69671122—
Edukt4-chloro-2-(2,6-dichlorophenyl)-2H-pyrazolo[4,3-c]pyridineHCID 86697036—
Produkt2-(2,6-Dichlorophenyl)-2h-pyrazolo[4,3-c]pyridin-4-amineHCID 6967117853%

Reaktionsschritte

Following the procedure described for N-[2-(2,6-dichlorophenyl)-2H-pyrazolo[4,3-c]pyridine-4-yl]-N′-methylpyrimidine-4,6-diamine, 4-chloro-2-(2,6-dichlorophenyl)-2H-pyrazolo[4,3-c]pyridine and 33% aqueous ammonia (1.5 mL) were reacted to afford the title compound as a white solid (139 mg, 53% yield). 1H NMR (400 MHz, DMSO-d6): δ 8.66 (d, J=0.9 Hz, 1H), 7.79-7.77 (m, 2H), 7.67 (dd, J=9.0, 7.3 Hz, 1H), 7.58 (d, J=6.5 Hz, 1H), 7.10 (br s, 2H), 6.74 (dd, J=6.5, 1.0 Hz, 1H). LCMS (Method B): RT=2.54 min, m/z: 279 [M+H+].

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09309240B2
Quelldatensatzuspto-grants-2016_04
ORD IDord-3416609ea71045369be752c1380bf9a6
Quellennotizuspto-grants-2016_04