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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1487409Erstellt: 24. Oktober 2026

Trifluoroacetic acid → HCID 89465782, Verbindung

https://huagongshe.com/de/reaction/1487409

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrifluoroacetic acidHCID 6422—
Edukt4-(4-Methylpiperazin-1-yl)benzaldehydeHCID 736533—
EduktSodium triacetoxyborohydrideHCID 5049666—
EduktHCID 178509236HCID 178509236—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 89465782HCID 89465782—

Reaktionsschritte

41.5 μl of trifluoroacetic acid (0.539 mmol) and, in small fractions, 129 mg (0.611 mmol) of sodium triacetoxyborohydride are added to a solution of 100 mg (0.35 mmol) of 5-(3,5-difluorophenylthio)-1H-pyrazolo[3,4-b]pyridin-3-amine and 81 mg (0.395 mmol) of 4-(4-methylpiperazin-1-yl)benzaldehyde in 20 ml of a 1:1 mixture of dichloromethane and tetrahydrofuran. The reaction medium is stirred for 16 hours at room temperature. An additional fraction of 125 μl of trifluoroacetic acid and 388 mg of sodium triacetoxyborohydride are added and the reaction medium is stirred for an additional 24 hours. The solvent is then concentrated and the reaction medium extracted with ethyl acetate and washed using saturated sodium bicarbonate solution. The organic phases are combined, dried on magnesium sulfate and then concentrated to yield a yellow oil. A trituration of this oil in methanol leads to the isolation of 135 mg of a yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09428510B2
Quelldatensatzuspto-grants-2016_08
ORD IDord-ac14a9ae3b4142e1aa07f635b74d4c56
Quellennotizuspto-grants-2016_08