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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1054024Erstellt: 26. Oktober 2026

Acetic Acid → 5-(1-Benzyl-piperidin-3-ylamino)-indazole-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1054024

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
Edukt1-Benzyl-3-piperidone hydrochloride hydrateHCID 3084924—
EduktSodium triacetoxyborohydrideHCID 5049666—
Edukt1,1-Dimethylethyl 5-amino-1H-indazole-1-carboxylateHCID 19800556—
Lösungsmittel1,2-DichloroethaneHCID 11—
LösungsmittelDichloromethaneHCID 6344—
Produkt5-(1-Benzyl-piperidin-3-ylamino)-indazole-1-carboxylic acid tert-butyl esterHCID 7097924275%

Reaktionsbedingungen

Temperatur30 °C

Reaktionsschritte

A mixture of 1-benzyl-piperidin-3-one hydrochloride (116 g, 0.52 mol, 1.2 eq) and TEA (43.5 g, 0.43 mol, 1.0 eq) in DCE (800 mL) was stirred at 30° C. for 1 hour. Then 5-amino-indazole-1-carboxylic acid tert-butyl ester (100 g, 0.43 mol, 1.0 eq) and CH3COOH (25.8 g, 0.43 mol, 1.0 eq) were added and the reaction mixture stirred for 30 min. NaBH(OAc)3 (273 g, 1.29 mol, 3.0 eq) was then added in one portion and the mixture stirred at 30° C. for 16 hours. LC-MS showed complete conversion. The reaction mixture was diluted in DCM (1 L) and the organic layer washed with saturated NaHCO3 (800 mL×3) and H2O (500 mL×3), dried over Na2SO4 and concentrated under vacuum. The crude product was purified by column chromatography on silica gel using (DCM:MeOH=60:1) to give the 5-(1-benzyl-piperidin-3-ylamino)-indazole-1-carboxylic acid tert-butyl ester (131 g, 75%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09394286B2
Quelldatensatzuspto-grants-2016_07
ORD IDord-ddb46d42fcd240a89dedebb92b1c59a3
Quellennotizuspto-grants-2016_07