Cesium carbonate → HCID 68817414, compound
Reaction equation
[CH3:1][O:2][C:3]([C:5]1[CH:10]=[C:9](Cl)[N:8]=[C:7]([C:12]([O:14][CH2:15][CH3:16])=[O:13])[CH:6]=1)=[O:4].C1(P(C2C=CC=CC=2)C2C=CC3C(=CC=CC=3)C=2C2C3C(=CC=CC=3)C=CC=2P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C(=O)([O-])[O-].[Cs+].[Cs+].[C@@H:69]([NH2:73])([CH2:71][CH3:72])[CH3:70]>C1(C)C=CC=CC=1.C([O-])(=O)C.[Pd+2].C([O-])(=O)C>[CH3:1][O:2][C:3]([C:5]1[CH:10]=[C:9]([NH:73][C@H:69]([CH2:71][CH3:72])[CH3:70])[N:8]=[C:7]([C:12]([O:14][CH2:15][CH3:16])=[O:13])[CH:6]=1)=[O:4]Participants
7
Conditions
- Temperature
- 80 °C
Procedure
Add 6-chloropyridine-2,4-dicarboxylic acid 2-ethyl ester 4-methyl ester (2.44 g, 10 mmol), palladium acetate (224 mg, 1.0 mmol), racemic-2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (623 mg, 1.0 mmol), cesium carbonate (4.95 g, 15.2 mmol) in toluene (70 mL) in a sealed tube. Degas the tube for 5 min with nitrogen, add (S)-sec-butylamine (1.2 mL, 11.8 mmol) and seal the tube. Heat to 80° C. overnight. Cool to room temperature and filter the mixture through a filtering agent. Wash with ethyl acetate. Dissolve the solid in water and extract with ethyl acetate. Combine all organic solutions, concentrate and purify (silica gel chromatography, eluting with ethyl acetate and hexanes) to give the title compound (2.5 g, 90%).
Workup
- customDegas the tube for 5 min with nitrogen
- customseal the tube
- temperatureCool to room temperature
- filtrationfilter the mixture through a filtering agent
- washWash with ethyl acetate
- dissolutionDissolve the solid in water
- extractionextract with ethyl acetate
- concentrationCombine all organic solutions, concentrate
- custompurify
- wash(silica gel chromatography, eluting with ethyl acetate and hexanes)
Sources & evidence
- ORD record
- ord-e397239ad0574202be74447576a6a575
- Source dataset
- uspto-grants-2009_09
- Patent number
- US07585885B2
Reaction notes
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