Top 5 Predictions Over IPI-145 This Coming Year

De Les Feux de l'Amour - Le site Wik'Y&R du projet Y&R.
Version du 13 octobre 2016 à 11:30 par Butane3area (discuter | contributions)

(diff) ← Version précédente | Voir la version courante (diff) | Version suivante → (diff)

The product was collected by filtration, washed with water and purified by crystallization from CH 2Cl 2/EtOH; yield 5.8 g (69%); 1H NMR (500 MHz, CDCl 3): �� = 8.35 (s, 1 H), 7.96 (dd, J=9.1, 3.0 Hz, 1 H), 7.73 (d, J=9.1 Hz, 1 H), 7.68 (d, J=9.1 Hz, 1 H), 6.93 (dd, J=9.1, 3.0 Hz, 1 H), 6.77 (s, 1 H), 3.03 (t, J=7.5 Hz, 2 H), 2.97 (s, 6 H), 1.77 (quin, J=7.5 Hz, 2 H), 1.26 (m, 16 H), 0.88 (t, J=7.5 Hz, 3 H). M-laurdan: MeNH 2?HCl (9.0 g, 0.13 IPI-145 cost mol) was added to a mixture of 2-hydroxy-6-dodecanoylnaphthalene (8.0 g, 26 mmol), Na 2S 2O 5 (12 g, 61 mmol), NaOH (5.2 g, 0.13 mol), and H 2O (100 ml) in a pressure tube and the mixture was stirred at 140��C for 48 h. The product was collected by filtration, washed with water and purified by crystallization from CH 2Cl 2/EtOH; yield 5.6 g (67%); 1H NMR (500 MHz, CDCl 3): �� = 8.33 (s, 1 H), 7.95 (dd, J=9.1, 3.0 Hz, 1 H), 7.74 (d, J=9.1 Hz, 1 H), 7.66 (d, J=9.1 Hz, 1 H), 7.29 www.selleckchem.com/CFTR.html (s, 1 H), 6.91 (dd, J=9.1, 3.0 Hz, 1 H), 6.77 (s, 1 H), 3.03 (t, J=7.5 Hz, 2 H), 2.97 (s, 3H), 1.77 (quin, J=7.5 Hz, 2 H), 1.26 (m, 16 H), 0.88 (t, J=7.5 Hz, 3 H). C-laurdan: A mixture of 6-dodecanoyl-2-(methylamino) naphthalene (3.0 g, 8.8 mmol), methyl bromoacetate (2.0 g, 13 mmol), Na 2HPO 4 (1.9 g, 13 mmol) and NaI (0.5 g, 3.5 mmol) in MeCN (50 ml) was refluxed under N 2 for 18 h. The product was extracted with ethyl acetate, washed with brine and purified by crystallization from EtOH to obtain a light yellow powder; yield 2.5 g (70%); 1H NMR (500 MHz, CDCl 3): �� = 8.35 (s, 1 H), 7.93 (dd, J=9.0, 3.0 Hz, 1 H), 7.82 (d, J=9.0 Hz, 1 H), 7.68 (d, J=9.0 Hz, 1 H), 7.08 (dd, J=9.0, 3.0 Hz, 1 H), 6.83 (s, 1 H), 4.23 (s, 2 H), 3.72 (s, 3H), 3.24 (s, 3 H), 3.04 (t, J=7.5 Hz, 2 H), 1.77 (quin, J=7.5 Hz, 2 H), 1.28 (m, 16 H), 0.89 (t, J=7.5 Hz, 3 H); A mixture of this intermediate (2.0 g, 4.9 Casein kinase 1 mmol) and KOH (0.70 g, 12 mmol) in EtOH (50 ml) was stirred for 5 h. The resultant solution was diluted with ice-water (100 ml) and concentrated HCl (aq) was added slowly at

Outils personnels