Reaktion #2161281

ord-24cdabd490a0486492d88726268a0f88

Reaktionsgleichung

Fc1ccc(Cc2cc(-c3ccncc3)nn2C2CNC2)cc1
4-(5-(4-fluorobenzyl)-1-(azetidin-3-yl)-1H-pyrazol-3-yl)pyridine
CCC(=O)Cl
propionyl chloride
CCN(CC)CC
triethylamine
CCC(=O)N1CC(n2nc(-c3ccncc3)cc2Cc2ccc(F)cc2)C1
title compound
CCC(=O)N1CC(n2nc(-c3ccncc3)cc2Cc2ccc(F)cc2)C1
1-(3-(5-(4-fluorobenzyl)-3-(pyridin-4-yl)-1H-pyrazol-1-yl)azetidin-1-yl)propan-1-one

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigepurified by flash chromatography (0-5% MeOH/CH2Cl2)

Vorschrift

To a solution of 4-(5-(4-fluorobenzyl)-1-(azetidin-3-yl)-1H-pyrazol-3-yl)pyridine (75 mg, 0.24 mmol) in CH2Cl2 (2 mL) was added propionyl chloride (22 μL, 0.24 mmol) and triethylamine (37 μL, 0.26 mmol) and the reaction mixture was stirred at room temperature for 2 hours. The solution was then loaded directly onto a pre-wetted Biotage 25M column and purified by flash chromatography (0-5% MeOH/CH2Cl2) to give the title compound as a white solid, 68 mg, 78%. 1H NMR (400 MHz, DMSO-D6) δ ppm 8.57 (d, 2 H), 7.74 (d, 2 H), 7.26 (t, 2 H), 7.16 (t, 2 H), 6.72 (s, 1 H), 5.25-5.34 (m, 1 H), 4.32-4.45 (m, 2 H), 4.07-4.13 (m, 4 H), 2.09 (q, 2 H), 0.97 (t, 3 H); m/z (APCI+) for C21H21N4FO 365.1 (M+H)+.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07919488B2uspto-grants-2011_04