HCID 21918625, compound → HCID 21918702, compound
Reaction equation
[CH3:1][C:2]([C:5]1[CH:6]=[C:7]([NH:16][C:17]([NH:19][CH2:20][C:21]2[CH:26]=[CH:25][C:24]([N+:27]([O-])=O)=[CH:23][CH:22]=2)=[O:18])[CH:8]=[C:9]([C:12]([CH3:15])([CH3:14])[CH3:13])[C:10]=1[OH:11])([CH3:4])[CH3:3]>C(O)C.C(OCC)(=O)C.[Pd]>[NH2:27][C:24]1[CH:25]=[CH:26][C:21]([CH2:20][NH:19][C:17]([NH:16][C:7]2[CH:6]=[C:5]([C:2]([CH3:1])([CH3:3])[CH3:4])[C:10]([OH:11])=[C:9]([C:12]([CH3:15])([CH3:14])[CH3:13])[CH:8]=2)=[O:18])=[CH:22][CH:23]=1Participants
5
Reactant 1
Product 1
Reagents, catalysts & solvents 3
Procedure
In a 100 ml autoclave, 0.55 g (1.38 mmole) of N-[3,5-bis-(1,1-dimethylethyl)-4-hydroxyphenyl]-N′-[(4-nitrophenyl)methyl]-urea is dissolved in a 2/1 mixture of ethanol and ethyl acetate, in the presence of 10% Pd/C. After hydrogenation for one and a half hours at 20° C., under 20 PSI, the mixture is filtered on celite and the filtrate is concentrated under vacuum. The evaporation residue is diluted in 20 ml of diethyl ether and the expected product crystallizes spontaneously. The crystals are filtered out and rinsed with 20 ml of diethyl ether. A white powder is obtained with a yield of 60% (0.31 g). Melting point: 194-195° C.
Workup
- waitAfter hydrogenation for one and a half hours at 20° C.
- filtrationunder 20 PSI, the mixture is filtered on celite
- concentrationthe filtrate is concentrated under vacuum
- additionThe evaporation residue is diluted in 20 ml of diethyl ether
- customthe expected product crystallizes spontaneously
- filtrationThe crystals are filtered out
- washrinsed with 20 ml of diethyl ether
- customA white powder is obtained with a yield of 60% (0.31 g)
Sources & evidence
- ORD record
- ord-fb417ccc27434012819a6a9257d0a239
- Source dataset
- uspto-grants-2008_12
- Patent number
- US07459558B2
Reaction notes
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