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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1911887Erstellt: 26. Oktober 2026

Acetic Acid → 2,2-Dimethyl-1-(5-(1-(4-(methylthio)benzyl)piperidin-3-ylamino)-1H-indazol-1-yl)propan-1-one

https://huagongshe.com/reaction/1911887

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
Edukt4-(Methylthio)benzaldehydeHCID 76985—
EduktSodium triacetoxyborohydrideHCID 5049666—
Edukt2,2-Dimethyl-1-(5-(piperidin-3-ylamino)-1H-indazol-1-yl)propan-1-oneHCID 59799768—
Lösungsmittel1,2-DichloroethaneHCID 11—
Produkt2,2-Dimethyl-1-(5-(1-(4-(methylthio)benzyl)piperidin-3-ylamino)-1H-indazol-1-yl)propan-1-oneHCID 5979977571,6%

Reaktionsschritte

Into a 25 mL round bottom flask were combined 2,2-dimethyl-1-(5-(piperidin-3-ylamino)-1H-indazol-1-yl)propan-1-one (0.250 g, 0.8 mmol), 1,2-dichloroethane (5 mL), 4-(methylthio)benzaldehyde (0.127 g, 0.8 mmol), glacial acetic acid (50 μL, 0.8 mmol), and sodium triacetoxyborohydride (0.229 g, 1.1 mmol). The reaction was evacuated and refilled with nitrogen. The reaction was monitored by HPLC and was complete upon the disappearance of the starting amine. The reaction was diluted with saturated sodium bicarbonate (10 mL) and dichloromethane (5 mL). After mixing, the organic phase was isolated, dried over MgSO4, filtered and concentrated to give the crude product. Chromatography of the residue on silica gel gave the title compound as an off-white solid (250 mg, 69%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08604205B2
Quelldatensatzuspto-grants-2013_12
ORD IDord-afe4c344dfb049968d0d51577582376a
Quellennotizuspto-grants-2013_12