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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 713461Erstellt: 26. Oktober 2026

(4-Ethoxy-3-fluorophenyl)boronic acid → 1,1-Dimethylethyl 4-(4-ethoxy-3-fluorobenzoyl)-1-piperidinecarboxylate

https://huagongshe.com/reaction/713461

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt(4-Ethoxy-3-fluorophenyl)boronic acidHCID 2782821—
Edukt4-Phenylsulfanylcarbonyl-piperidine-1-carboxylic acid tert-butyl esterHCID 89375800—
KatalysatorBis(dibenzylideneacetone)palladiumHCID 9811564—
KatalysatorCuprous 2-thiophenecarboxylateHCID 11194830—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1,1-Dimethylethyl 4-(4-ethoxy-3-fluorobenzoyl)-1-piperidinecarboxylateHCID 7122678282,6%

Reaktionsschritte

To a mixture of 4-ethoxy-3-fluorophenylboronic acid (0.86 g, 4.67 mmol), ligand TFP (0.144 g, 0.62 mmol), Pd2dba3 (0.29 g, 0.31 mmol), copper (I) thiophene-2-carboxylate (0.89 g, 4.7 mmol) was added a solution of 4-phenylsulfanylcarbonyl-piperidine-1-carboxylic acid tert-butyl ester (1.0 g, 3.11 mmol) in 10 mL of THF while purging with N2 at 50° C. After 18 hours the reaction mixture was diluted with ethyl acetate, filtered through celite then concentrated in vacuo. Purification by flash chromatography gave the title compound (0.95 g, 2.57 mmol). MS (ESI) m/z 352.0 (M+H+); HPLC (Novapak 150×3.9 mm C-18 column: mobile phase: 35-90% acetonitrile/water with 0.1% TFA, at 2 mL/min over 2 min.) t 1.42 min.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09181266B2
Quelldatensatzuspto-grants-2015_11
ORD IDord-d0bd7f4aa1404a8b81ccc81c987bd368
Quellennotizuspto-grants-2015_11