HCID 136340575, compound → HCID 136340576, compound
Reaction equation
[N+:1]([C:4]1[CH:50]=[CH:49][C:7]([O:8][C:9]2[CH:10]=[C:11]([C:15]3[O:19][C:18]([C:20]4[CH:25]=[C:24]([OH:26])[C:23]([C:27]5[O:28][C:29]([C:32]6[CH:37]=[CH:36][CH:35]=[C:34]([O:38][C:39]7[CH:44]=[CH:43][C:42]([N+:45]([O-])=O)=[CH:41][CH:40]=7)[CH:33]=6)=[N:30][N:31]=5)=[CH:22][C:21]=4[OH:48])=[N:17][N:16]=3)[CH:12]=[CH:13][CH:14]=2)=[CH:6][CH:5]=1)([O-])=O>C1COCC1.[Pd]>[NH2:1][C:4]1[CH:5]=[CH:6][C:7]([O:8][C:9]2[CH:10]=[C:11]([C:15]3[O:19][C:18]([C:20]4[CH:25]=[C:24]([OH:26])[C:23]([C:27]5[O:28][C:29]([C:32]6[CH:37]=[CH:36][CH:35]=[C:34]([O:38][C:39]7[CH:44]=[CH:43][C:42]([NH2:45])=[CH:41][CH:40]=7)[CH:33]=6)=[N:30][N:31]=5)=[CH:22][C:21]=4[OH:48])=[N:17][N:16]=3)[CH:12]=[CH:13][CH:14]=2)=[CH:49][CH:50]=1Participants
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
0.30 g of 2,5-bis(5-(3-(4-nitrophenoxy)phenyl)-1,3,4-oxadiazole-2-yl)benzene-1,4-diol prepared in Synthesis Example 15 was dissolved in 150 ml of THF, and 0.05 g of a catalyst having 5 wt % of palladium impregnated in activated carbon was added thereto. Gases generated in the solution by purging an argon (Ar) gas were removed to create a vacuum, followed by stirring for 18 hours while supplying H2 gas (approximately 2-3 atm) for inducing a reaction. After the reaction was completed, the reaction product was filtered with Celite powder to remove the catalyst, and performing silica gel column chromatography (developed with a solution having ethylacetate:n-hexane mixed in a ratio of 1:2) to yield 0.1 g of a product having Formula 39. 1H NMR (300 MHz, CDCl3) analytical results of the product were as follows:
Workup
- additionwas added
- customby purging an argon (Ar) gas
- customwere removed
- customa reaction
- filtrationthe reaction product was filtered with Celite powder
- customto remove the catalyst
- additionn-hexane mixed in a ratio of 1:2)
Sources & evidence
- ORD record
- ord-fe6f4c32c657448d94cedf467952eeb3
- Source dataset
- uspto-grants-2015_05
- Patent number
- US09024036B2
Reaction notes
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