Reaktion #491

ord-b099625680284510ba7d7318538524ab

Reaktionsgleichung

CC(C)(C)OC(=O)c1ccc(Br)nc1
CC(C)(C)OC(=O)c1ccc(
C1CCNCC1
C1CCNCC1
CC(C)(C)OC(=O)c1ccc(N2CCCCC2)nc1
CC(C)(C)OC(=O)c1ccc(
Ausbeute 61.9%

Lösungsmittel

Reaktionsbedingungen

Temperatur
80°CELSIUS

Vorschrift

In a 100 mL round-bottomed flask was tert-butyl 6-bromonicotinate (516 mg, 2 mmol), piperidine (237 µl, 2.40 mmol), and CESIUM CARBONATE (977 mg, 3.00 mmol) in dioxane (9763 µl) to give a white suspension. The solution was degassed with N2 (g) fo 20 mins. PALLADIUM(II) ACETATE (22.45 mg, 0.10 mmol) and BINAP (62.3 mg, 0.10 mmol) were added under N2 (g) and the reaction was heated to 100 °C. Start Time: 01-Jul-10 1:10:32 PM -0400. The reaction was checked by LC-MS (complete), filtered, rinsed with DCM, concentrated in vacuo. _02 July 2010_ Purification by Iscos (25 g) using 100% Hexanes -> 50% EtOAc in Hexanes afforded a white solid. 325 mg obtained. 1H NMR (300 MHz, DMSO- _d_ 6) d ppm 1.51 - 1.57 (m, 12 H) 1.57 - 1.77 (m, 5 H) 3.58 - 3.74 (m, 4 H) 6.78 - 6.92 (m, 1 H) 7.88 (dd, _J_ =9.16, 2.36 Hz, 1 H) 8.60 (dd, _J_ =2.45, 0.57 Hz, 1 H). LC-MS: Rt = 2.37 min. Method: Short Purity. MS ES+: 263.2 [M+H]+.

Quelle

750 AstraZeneca ELN dataset