Potassium Carbonate → HCID 59314324, compound
Reaction equation
[CH2:1]([O:3][C:4]([C:6]1([NH:16][C:17](=[O:26])[C:18]2[CH:23]=[CH:22][CH:21]=[C:20]([CH3:24])[C:19]=2I)[CH2:14][C:13]2[C:8](=[CH:9][CH:10]=[C:11]([F:15])[CH:12]=2)[CH2:7]1)=[O:5])[CH3:2].C([O-])([O-])=O.[K+].[K+]>CCO.O1CCOCC1.[Pd]>[CH2:1]([O:3][C:4]([C:6]1([NH:16][C:17](=[O:26])[C:18]2[CH:23]=[CH:22][CH:21]=[C:20]([CH3:24])[C:19]=2[CH:4]=[C:6]([CH3:14])[CH3:7])[CH2:14][C:13]2[C:8](=[CH:9][CH:10]=[C:11]([F:15])[CH:12]=2)[CH2:7]1)=[O:5])[CH3:2]Participants
6
Procedure
To a solution of 5-fluoro-2-(2-iodo-3-methyl-benzoylamino)-indan-2-carboxylic acid ethyl ester (400 mg, 0.85 mmol) and 2,2-dimethyethylenelboronic acid (342 mg, 3.42 mmol) in EtOH (10 mL) and dioxane (5 mL) is added palladium anchored homogeneous catalyst, FibreCatPd(0) (4.84% Pd, 186 mg, 8.5% mmol) and 2M aqueous solution of K2SO4 (1.71 mL, 3.42 mmol). The resulting reaction mixture is covered with argon and run in a microwave reaction: 120° C., 7 h. After concentration in vacuo, the residue is purified by HPLC to give a pure product (148) as a colorless oil (245 mg, 73%).
Workup
- customThe resulting reaction mixture
- customrun in a microwave reaction
- custom120° C., 7 h
- concentrationAfter concentration in vacuo
- customthe residue is purified by HPLC
Sources & evidence
- ORD record
- ord-ddd73992bee34a5286b5c66d62d76e55
- Source dataset
- uspto-grants-2013_10
- Patent number
- US08569535B2
Reaction notes
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