Potassium Carbonate → 2-amino-N,N-dimethyl-5-[8-methyl-4-(4-pyridinyl)-6-quinolinyl]-3-pyridinesulfonamide
Reaction equation
Br[C:2]1[CH:3]=[C:4]2[C:9](=[C:10]([CH3:12])[CH:11]=1)[N:8]=[CH:7][CH:6]=[C:5]2Cl.B1(B2OC(C)(C)C(C)(C)O2)OC(C)(C)C(C)(C)O1.C([O-])(=O)C.[K+].[NH2:37][C:38]1[C:43]([S:44]([N:47]([CH3:49])[CH3:48])(=[O:46])=[O:45])=[CH:42][C:41](Br)=[CH:40][N:39]=1.C(=O)([O-])[O-].[K+].[K+].CC1(C)C(C)(C)OB([C:65]2[CH:70]=[CH:69][N:68]=[CH:67][CH:66]=2)O1>O1CCOCC1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.Cl[Pd]Cl.[Fe+2]>[NH2:37][C:38]1[C:43]([S:44]([N:47]([CH3:49])[CH3:48])(=[O:46])=[O:45])=[CH:42][C:41]([C:2]2[CH:3]=[C:4]3[C:9](=[C:10]([CH3:12])[CH:11]=2)[N:8]=[CH:7][CH:6]=[C:5]3[C:65]2[CH:70]=[CH:69][N:68]=[CH:67][CH:66]=2)=[CH:40][N:39]=1Participants
Reactant 6
Product 1
Reagents, catalysts & solvents 2
Procedure
A mixture of 6-bromo-4-chloro-8-methylquinoline (0.300 g, 1.170 mmol), bis(pinacolato)diboron (0.297 g, 1.170 mmol), dichloro[1,1′-bis(diphenylphosphino)ferrocene]palladium (II) dichloromethane adduct (0.029 g, 0.035 mmol), and solid anhydrous potassium acetate (0.459 g, 4.676 mmol) in dry 1,4-dioxane (8 mL) was heated at reflux for 70 minutes. The oil bath was temporarily removed and to the reaction was added 2-amino-5-bromo-N,N-dimethyl-3-pyridinesulfonamide (0.327 g, 1.17 mmol), dichloro[1,1′-bis(diphenylphosphino)ferrocene]palladium (II) dichloromethane adduct (0.047 g, 0.058 mmol), and 2 M aqueous potassium carbonate (0.646 g, 4.676 mmol, 2.34 mL). The reaction was heated at reflux for 80 minutes. The oil bath was temporarily removed and to the reaction was added 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine (0.240 g, 1.17 mmol), dichloro[1,1′-bis(diphenylphosphino)ferrocene]palladium (II) dichloromethane adduct (0.047 g, 0.058 mmol), 2 M aqueous potassium carbonate (0.485 g, 3.51 mmol, 1.76 mL), and 1,4-dioxane (6 mL). The reaction was heated at reflux for 17 h and concentrated in vacuo. The residue was triturated with 10% MeOH:EtOAc (45 mL), filtered through filter paper, and the filtrate was concentrated in vacuo. The residue was purified by flash chromatography on silica gel (7% MeOH:EtOAc) to give the title compound (0.135 g, 28%) as a yellow powder. MS (ES)+ m/e 420 [M+H].
Workup
- temperaturewas heated
- temperatureat reflux for 70 minutes
- customThe oil bath was temporarily removed and to the reaction
- temperatureThe reaction was heated
- temperatureat reflux for 80 minutes
- customThe oil bath was temporarily removed and to the reaction
- temperatureThe reaction was heated
- temperatureat reflux for 17 h
- concentrationconcentrated in vacuo
- customThe residue was triturated with 10% MeOH
- filtrationEtOAc (45 mL), filtered
- filtrationthrough filter paper
- concentrationthe filtrate was concentrated in vacuo
- customThe residue was purified by flash chromatography on silica gel (7% MeOH:EtOAc)
Sources & evidence
- ORD record
- ord-04430095f69649339473c41dc7b8b228
- Source dataset
- uspto-grants-2014_01
- Patent number
- US08633187B2
Reaction notes
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