HCID 23146835, compound → HCID 23146838, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[C:18]([C:19]3[CH:24]=[CH:23][C:22]([O:25][CH3:26])=[CH:21][CH:20]=3)=[N:17][C:16]3[C:11](=[CH:12][CH:13]=[CH:14][C:15]=3[NH:27][C:28]3[CH:33]=[CH:32][C:31]([N+:34]([O-])=O)=[CH:30][CH:29]=3)[N:10]=2)=[CH:5][CH:4]=1>O1CCCC1>[O:2]([C:3]1[CH:4]=[CH:5][C:6]([C:9]2[C:18]([C:19]3[CH:24]=[CH:23][C:22]([O:25][CH3:26])=[CH:21][CH:20]=3)=[N:17][C:16]3[C:11](=[CH:12][CH:13]=[CH:14][C:15]=3[NH:27][C:28]3[CH:29]=[CH:30][C:31]([NH2:34])=[CH:32][CH:33]=3)[N:10]=2)=[CH:7][CH:8]=1)[CH3:1]Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
8.3 g (17.3 mmol) of 2,3-di(4-methoxyphenyl)-5-(4-nitrophenyl)aminoquinoxaline was dissolved in 100 ml of tetrahydrofuran, and a reaction container was purged with nitrogen. Thereafter, 5.0 g of 5% Pd/C (hydrous) was added, followed by sufficient purging with nitrogen again. This system was purged with hydrogen, followed by reaction at room temperature for 10 hours. After completion of the reaction, the system was filtered, and the resulting filtration residue was washed with tetrahydrofuran and filtered again. The solvent was removed from the resulting filtrate, and a reaction product was recrystallized in hexane to obtain the intended product.
Workup
- customa reaction container was purged with nitrogen
- additionThereafter, 5.0 g of 5% Pd/C (hydrous) was added
- customby sufficient purging with nitrogen again
- customThis system was purged with hydrogen
- customfollowed by reaction at room temperature for 10 hours
- customAfter completion of the reaction
- filtrationthe system was filtered
- filtrationthe resulting filtration residue
- washwas washed with tetrahydrofuran
- filtrationfiltered again
- customThe solvent was removed from the resulting filtrate
- customa reaction product was recrystallized in hexane
- customto obtain the intended product
Sources & evidence
- ORD record
- ord-d10b38acf01445688ca9380d0d84db5b
- Source dataset
- uspto-grants-2010_09
- Patent number
- US07799894B2
Reaction notes
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