Pyridine → HCID 66747924, compound
Reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5](B(O)O)=[CH:4][CH:3]=1.[O:11]=[S:12]1(=[O:29])[CH2:17][CH2:16][N:15]2[CH2:18][CH2:19][CH2:20][CH:21]([C:22]3[CH:27]=[CH:26][C:25]([OH:28])=[CH:24][CH:23]=3)[C:14]2=[N:13]1.N1C=CC=CC=1.C(=O)([O-])[O-].[Cs+].[Cs+]>CS(C)=O.O.C(O[Cu]OC(=O)C)(=O)C>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([O:28][C:25]2[CH:24]=[CH:23][C:22]([CH:21]3[C:14]4=[N:13][S:12](=[O:29])(=[O:11])[CH2:17][CH2:16][N:15]4[CH2:18][CH2:19][CH2:20]3)=[CH:27][CH:26]=2)=[CH:4][CH:3]=1Participants
8
Reactant 4
Product 1
Reagents, catalysts & solvents 3
Procedure
A mixture of 4-chlorophenylboronic acid (167 mg), 4-(2,2-dioxido-3,4,6,7,8,9-hexahydropyrido[2,1-c][1,2,4]thiadiazin-9-yl)phenol (100 mg), pyridine (0.087 mL), diacetoxycopper (130 mg), and cesium carbonate (116 mg) in DMSO (3.0 mL) was stirred at room temperature for 24 hr. The mixture was diluted with water, and extracted with EtOAc (40 ml). The organic layer was washed with 0.1N NaOH aq. (2×40 ml) and then brine, dried over anhydrous magnesium sulfate, and concentrated in vacuo. The residue was purified by column chromatography (silica gel, eluted with MeOH in EtOAc) to give the title compound (23.0 mg) as a white solid.
Workup
- extractionextracted with EtOAc (40 ml)
- washThe organic layer was washed with 0.1N NaOH aq. (2×40 ml)
- dry with materialbrine, dried over anhydrous magnesium sulfate
- concentrationconcentrated in vacuo
- customThe residue was purified by column chromatography (silica gel, eluted with MeOH in EtOAc)
Sources & evidence
- ORD record
- ord-6a0ab46984c64e4ba2d3c66c16c5a976
- Source dataset
- uspto-grants-2014_07
- Patent number
- US08778934B2
Reaction notes
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