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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1362098Erstellt: 24. Oktober 2026

tert-Butyl acrylate → (E)-3-(6-Amino-5-piperidin-1-ylmethyl-pyridin-3-yl)acrylic acid tert-butyl ester

https://huagongshe.com/de/reaction/1362098

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukttert-Butyl acrylateHCID 15458—
EduktTri-o-tolylphosphineHCID 80271—
EduktDiisopropylethylamineHCID 81531—
Edukt5-Bromo-3-piperidin-1-ylmethyl-pyridin-2-ylamineHCID 59456983—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelPropionitrileHCID 7854—
Produkt(E)-3-(6-Amino-5-piperidin-1-ylmethyl-pyridin-3-yl)acrylic acid tert-butyl esterHCID 5945693160%

Reaktionsschritte

A solution of 5-bromo-3-piperidin-1-ylmethyl-pyridin-2-ylamine (500 mg, 1.85 mmol), tert-butyl acrylate (0.3 mL, 2.0 mmol), (i-Pr)2EtN (0.5 mL, 2.8 mmol) and P(o-tol)3 (114 mg, 0.37 mmol) in EtCN (10 mL) was de-oxygenated with argon for 30 min. Pd(OAc)2 (43 mg, 0.19 mmol) was added, and the mixture was de-oxygenated for 15 min. The mixture was heated to reflux for 18 h and then allowed to cool. The solvent was removed in vacuo. The residue was partitioned between EtOAc and H2O. The organic layer was washed with H2O and satd NaCl, dried over Na2SO4 and concentrated. Purification by column chromatography (silica gel, CH2Cl2 to 96:4 CH2Cl2/CH3OH) gave the title compound (350 mg, 60%) as a yellow solid: MS (ESI) m/e 318 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07879872B2
Quelldatensatzuspto-grants-2011_02
ORD IDord-5ba8fdefc565475a8d58ef676427d959
Quellennotizuspto-grants-2011_02