Cesium carbonate → HCID 58066681, compound
Reaction equation
[NH:1]1[CH:5]=[C:4]([CH2:6][C:7]#[N:8])[CH:3]=[N:2]1.Br[CH2:10][C:11]1[CH:16]=[CH:15][C:14]([NH:17][C:18](=[O:23])[C:19]([CH3:22])([CH3:21])[CH3:20])=[CH:13][C:12]=1[CH2:24][S:25][C:26]([CH3:29])([CH3:28])[CH3:27].C(=O)([O-])[O-].[Cs+].[Cs+]>CC#N>[C:26]([S:25][CH2:24][C:12]1[CH:13]=[C:14]([NH:17][C:18](=[O:23])[C:19]([CH3:22])([CH3:21])[CH3:20])[CH:15]=[CH:16][C:11]=1[CH2:10][N:1]1[CH:5]=[C:4]([CH2:6][C:7]#[N:8])[CH:3]=[N:2]1)([CH3:29])([CH3:28])[CH3:27]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
(1H-Pyrazol-4-yl)-acetonitrile (0.19 g, 1.77 mmol) and N-(4-bromomethyl-3-tert-butylsulfanylmethyl-phenyl)-2,2-dimethyl-propionamide (0.20 g, 0.55 mmol) were combined in MeCN. Cesium carbonate (0.95 g, 2.90 mmol) was added, and the reaction was stirred for 45 minutes at room temperature. The mixture was worked-up and purified by silica gel chromatography to give the title compound.
Workup
- custompurified by silica gel chromatography
Sources & evidence
- ORD record
- ord-5d951142a32340fa98a32ed337862b90
- Source dataset
- uspto-grants-2013_02
- Patent number
- US08383654B2
Reaction notes
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