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HRID 243021Erstellt: 26. Oktober 2026

Sodium Iodide → 2,2-Dimethylpropionic acid 2-((R)-3-tert-butoxycarbonylaminopiperidin-1-yl)ethyl ester

https://huagongshe.com/reaction/243021

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium IodideHCID 5238—
EduktPotassium CarbonateHCID 11430—
Edukt(3R)-3-Aminopiperidine, 3-BOC protectedHCID 1514172—
Edukt2-Bromoethyl 2,2-dimethylpropanoateHCID 14572204—
LösungsmittelDimethylformamideHCID 6228—
Produkt2,2-Dimethylpropionic acid 2-((R)-3-tert-butoxycarbonylaminopiperidin-1-yl)ethyl esterHCID 6815797088%

Reaktionsschritte

A mixture of 2,2-dimethylpropionic acid 2-bromoethyl ester (2.3 g, 11 mmol), (R)-piperidin-3-ylcarbamic acid tert-butyl ester (2 g, 10.0 mmol), potassium carbonate (4.15 g, 30 mmol) and sodium iodide (0.15 g, 1 mmol) in DMF (20 mL) was stirred at RT for 2 days. The reaction mixture was partitioned between water and EtOAc. The aqueous phase was extracted with EtOAc and the combined organic fractions washed with water, followed by brine, then dried (Na2SO4) and concentrated in vacuo. The resulting residue was purified by column chromatography (Si—PCC, eluant 10-40% EtOAc in cyclohexane) affording the title compound as a colourless oil (2.884 g, 88%). 1H NMR (CDCl3, 300 MHz): 5.09 (1H, bs), 4.25-4.07 (2H, m), 3.73 (1H, bs), 2.63-2.52 (3H, m), 2.49 (1H, bs), 2.31-2.24 (1H, m), 1.74-1.61 (1H, m), 1.59-1.49 (3H, m), 1.44 (9H, s), 1.21 (9H, s).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08653089B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-275f098771fd4e269bc1b54cbb1fbcda
Quellennotizuspto-grants-2014_02