Water → HCID 18752900, compound
Reaction equation
Br[C:2]1[C:3]([NH2:9])=[N:4][CH:5]=[C:6]([Cl:8])[CH:7]=1.[O:10]1[C:14]2[CH:15]=[CH:16][C:17](/[CH:19]=[CH:20]/[Sn](CCCC)(CCCC)CCCC)=[CH:18][C:13]=2[O:12][CH2:11]1.C1(C)C=CC=CC=1P(C1C=CC=CC=1C)C1C=CC=CC=1C.O>CN(C=O)C.C(N(CC)CC)C.C([O-])(=O)C.[Pd+2].C([O-])(=O)C>[O:10]1[C:14]2[CH:15]=[CH:16][C:17](/[CH:19]=[CH:20]/[C:2]3[C:3]([NH2:9])=[N:4][CH:5]=[C:6]([Cl:8])[CH:7]=3)=[CH:18][C:13]=2[O:12][CH2:11]1Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 3
Procedure
A solution of 3-bromo-5-chloro-2-pyridinamine (318 mg, 1.5 mmol), [(E)-2-(1,3-benzodioxol-5-yl)ethenyl](tributyl)stannane (250 mg, 1.7 mmol) (A. J. Bridges, A. Lee, C. E. Schwatrz, M. J. Towle, B. A. Littlefield, Bioorg. Med. Chem., 1993, 1, 403), palladium acetate (19 mg, 0.08 mmol) and tri-o-tolylphosphine (50 mg, 0.16 mmol) in DMF (0.5 ml) and triethylamine (0.5 ml) in a teflon pressure vessel was heated in a microwave (full power) for 20 sec, allowed to cool to RT heated in a microwave for a further 20 sec and then 1 min 20 sec. After allowing to cool, the reaction mixture was poured into water (20 ml) and extracted with EtOAc (3×20 ml). The combined extracts were washed with water (2×20 ml), dried over MgSO4 and concentrated. Recrystallisation from EtOAc—hexane gave the title compound as a brown solid (170 mg, 0.6 mmol):
Workup
- temperatureheated in a microwave for a further 20 sec
- custom1 min 20 sec
- temperatureto cool
- extractionextracted with EtOAc (3×20 ml)
- washThe combined extracts were washed with water (2×20 ml)
- dry with materialdried over MgSO4
- concentrationconcentrated
- customRecrystallisation from EtOAc—hexane
Sources & evidence
- ORD record
- ord-8af0a66f73f94494bb11ee15c44d86ed
- Source dataset
- uspto-grants-2003_06
- Patent number
- US06583162B1
Reaction notes
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