Reaction equation
Cl[C:2]1[N:7]=[C:6]([NH2:8])[CH:5]=[CH:4][N:3]=1.[CH2:9](B(CC)CC)[CH3:10].[O-]P([O-])([O-])=O.[K+].[K+].[K+].O>C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.Cl[Pd]Cl.[Fe+2].O1CCCC1>[CH2:9]([C:2]1[N:7]=[C:6]([NH2:8])[CH:5]=[CH:4][N:3]=1)[CH3:10]Participants
7
Reactant 4
Product 1
Reagents, catalysts & solvents 2
Procedure
A 100-mL single-neck round-bottomed flask equipped with a magnetic stirrer and a reflux condenser was charged with 2-chloropyrimidin-4-amine (2.60 g, 20.0 mmol), triethylborane (20.0 mL, 1.0 M in THF, 20.0 mmol), Pd(dppf)Cl2 (816 mg, 1.0 mmol), K3PO4 (13.0 g, 40.0 mmol), water (2 mL), and tetrahydrofuran (50 mL). After three cycles of vacuum/argon flush, the mixture was heated at reflux for 14 h. It was then cooled to room temperature and filtered. The filtrate was concentrated under reduced pressure and the resulting residue was purified by silica-gel column chromatography eluting with 40:1 dichloromethane/methanol to afford 229a as yellow solid (600 mg, 24%). MS-ESI: [M+H]+ 124.3
Workup
- customA 100-mL single-neck round-bottomed flask equipped with a magnetic stirrer and a reflux condenser
- customAfter three cycles of vacuum/argon flush
- temperaturethe mixture was heated
- temperatureat reflux for 14 h
- filtrationfiltered
- concentrationThe filtrate was concentrated under reduced pressure
- customthe resulting residue was purified by silica-gel column chromatography
- washeluting with 40:1 dichloromethane/methanol
Sources & evidence
- ORD record
- ord-bc12d6b4019e45538053503a395015a9
- Source dataset
- uspto-grants-2016_01
- Patent number
- US09238655B2
Linked notes
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