Cesium carbonate → 5-phenyl-1H-indole-7-carboxylic acid
Reaction equation
Br[C:2]1[CH:3]=[C:4]2[C:8](=[C:9]([C:11]([OH:13])=[O:12])[CH:10]=1)[NH:7][CH:6]=[CH:5]2.[C:14]1(B(O)O)[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1.C(=O)([O-])[O-].[Cs+].[Cs+].[Cl-].CC1C=C(C)C=C(C)C=1[N+]1C=CN(C2C(C)=CC(C)=CC=2C)C=1>O1CCOCC1.O.C([O-])(=O)C.[Pd+2].C([O-])(=O)C>[C:14]1([C:2]2[CH:3]=[C:4]3[C:8](=[C:9]([C:11]([OH:13])=[O:12])[CH:10]=2)[NH:7][CH:6]=[CH:5]3)[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 3
Procedure
To a solution of 5-bromo-1H-indole-7-carboxylic acid (10 g, 41.8 mmol) in dioxane (150 mL) and water (50 mL) was added phenylboronic acid (19.5 g, 159.9 mmol), cesium carbonate (26.0 g, 79.8 mmol), 1,3-Bis(2,4,6-trimethylphenyl) imidazolium chloride (2.8 g, 8.2 mmol), and palladiumacetate (0.9 g, 4.01 mmol). The reaction mixture was stirred at ambient temperature for 15 min, and then was refluxed at 80° C. for 15 hr. The organic solvent was removed under reduced pressure and the water layer was adjusted to pH=1-2 with 6 M hydrochloric acid before ethyl acetate (350 mL) was added into it. The organic layer washed with water (100 mL×3), dried and concentrated at 45° C. to a thick oil (approximately 40 mL solvent left), cooled to −20° C., and filtered. The solid was washed with cold ethyl acetate (10 mL×3), and collected. The filtrate was concentrated to a thick oil at 45° C., then was cooled to −20° C., and off-white solid was obtained. The suspension was filtered and washed with cold ethyl acetate (5 mL×3). The filtrate was discard after 3 iterations of the above procedure.
Workup
- temperaturewas refluxed at 80° C. for 15 hr
- customThe organic solvent was removed under reduced pressure
- additionwas added into it
- washThe organic layer washed with water (100 mL×3)
- customdried
- concentrationconcentrated at 45° C. to a thick oil (approximately 40 mL solvent left)
- temperaturecooled to −20° C.
- filtrationfiltered
- washThe solid was washed with cold ethyl acetate (10 mL×3)
- customcollected
- concentrationThe filtrate was concentrated to a thick oil at 45° C.
- temperaturewas cooled to −20° C.
- customoff-white solid was obtained
- filtrationThe suspension was filtered
- washwashed with cold ethyl acetate (5 mL×3)
Sources & evidence
- ORD record
- ord-4aaf1123c6fc4b40b87f539300a8529b
- Source dataset
- uspto-grants-2010_12
- Patent number
- US07858796B2
Reaction notes
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