Cesium carbonate → HCID 59556892, compound
Reaction equation
[CH3:1][O:2][CH2:3][CH:4]1[NH:8][C:7](=[O:9])[C:6]([CH3:11])([CH3:10])[C:5]1=[O:12].Br[C:14]1[CH:21]=[CH:20][C:17]([C:18]#[N:19])=[C:16]([Cl:22])[CH:15]=1.C(=O)([O-])[O-].[Cs+].[Cs+].C1(P(C2C=CC=CC=2)C2C3OC4C(=CC=CC=4P(C4C=CC=CC=4)C4C=CC=CC=4)C(C)(C)C=3C=CC=2)C=CC=CC=1>C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.[Pd].[Pd]>[Cl:22][C:16]1[CH:15]=[C:14]([N:8]2[CH:4]([CH2:3][O:2][CH3:1])[C:5](=[O:12])[C:6]([CH3:10])([CH3:11])[C:7]2=[O:9])[CH:21]=[CH:20][C:17]=1[C:18]#[N:19]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
Using 5-(methoxymethyl)-3,3-dimethylpyrrolidine-2,4-dione (700 mg), 4-bromo-2-chlorobenzonitrile (1.06 g), cesium carbonate (2.00 g), tris(dibenzylideneacetone)dipalladium(0) (187 mg) and 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (355 mg), and in the same manner as in Reference Example 3, the title compound was obtained as colorless crystals (yield: 219 mg, 17%).
Sources & evidence
- ORD record
- ord-93f94095224d4b2ab216f40389d7e590
- Source dataset
- uspto-grants-2010_11
- Patent number
- US07834051B2
Reaction notes
Loading…