تفاعل #172710

معادلة التفاعل

6-Bromo-1-(1-methylethyl)-N-[(6-methyl-2-oxo-4-phenyl-1,2-dihydro-3-pyridinyl)methyl]-1H-indazole-4-carboxamide

hydrogen

reactin

→

title compound

المردود 37.0%

1-(1-Methylethyl)-N-[(6-methyl-2-oxo-4-propyl-1,2-dihydro-3-pyridinyl)methyl]-1H-indazole-4-carboxamide

المردود 37.0%

المذيبات

EtOH THF

ظروف التفاعل

المعالجة

1. 1
   ترشيحIt was filtered through Celite
2. 2
   غسيلwashed with EtOAc and EtOH
3. 3
   أخرىthe solvent was evaporated
4. 4
   workup.ADDITIONDMF was added with some water and white solids
5. 5
   ترشيحthat crashed out were filtered off
6. 6
   أخرىair-dried for 15 min
7. 7
   أخرىdried in a vacuum oven for 3 h
8. 8
   أخرىThe residue was purified by Gilson reversed-phase HPLC (30×100 Varian Polaris C18, 15-80% gradient of MeCN in water with 0.1% TFA over 12 minutes)
9. 9
   أخرىMost of the solvent was removed
10. 10
    workup.ADDITIONsaturated NaHCO3 was added
11. 11
    ترشيحThe solids that crashed out were filtered off
12. 12
    أخرىair-dried for 15 min
13. 13
    أخرىdried in vacuum oven overnight

الإجراء التجريبي

6-Bromo-1-(1-methylethyl)-N-[(6-methyl-2-oxo-4-phenyl-1,2-dihydro-3-pyridinyl)methyl]-1H-indazole-4-carboxamide (70.3 mg, 0.15 mmol) in 3:1 EtOH/THF (4 mL) was hydrogenated using Pd/C (10% wet Degussa type) and a balloon of hydrogen. The reactin mixture was stirred at room temperature overnight. It was filtered through Celite, washed with EtOAc and EtOH and the solvent was evaporated. DMF was added with some water and white solids that crashed out were filtered off, air-dried for 15 min and dried in a vacuum oven for 3 h. The residue was purified by Gilson reversed-phase HPLC (30×100 Varian Polaris C18, 15-80% gradient of MeCN in water with 0.1% TFA over 12 minutes). Most of the solvent was removed and saturated NaHCO3 was added. The solids that crashed out were filtered off, air-dried for 15 min and dried in vacuum oven overnight to give the title compound (19 mg, 37%). 1H NMR (400 MHz, DMSO-d6) δ ppm 11.75 (br. s., 1H) 8.63 (br. s., 1H) 8.34 (s, 1H) 7.85 (d, J=8.34 Hz, 1H) 7.39-7.51 (m, 7H) 5.99 (s, 1H) 5.03 (quin, J=6.57 Hz, 1H) 4.22 (d, J=4.29 Hz, 2H) 2.21 (s, 3H) 1.49 (s, 3H) 1.47 (s, 3H). MS(ES) [M+H]+ 367.2.

المصدر