HCID 19855899, compound → HCID 19855943, compound
Reaction equation
[ClH:1].[F:2][C:3]1[CH:8]=[CH:7][C:6]([N:9]([CH2:23][CH2:24][N:25]([CH2:33][CH2:34][C:35]2[CH:40]=[CH:39][CH:38]=[CH:37][CH:36]=2)CC2C=CC=CC=2)[C:10](=[O:22])[C:11]2[CH:16]=[CH:15][C:14]([NH:17][S:18]([CH3:21])(=[O:20])=[O:19])=[CH:13][CH:12]=2)=[CH:5][CH:4]=1>[Pd].C(O)C>[ClH:1].[F:2][C:3]1[CH:4]=[CH:5][C:6]([N:9]([CH2:23][CH2:24][NH:25][CH2:33][CH2:34][C:35]2[CH:36]=[CH:37][CH:38]=[CH:39][CH:40]=2)[C:10](=[O:22])[C:11]2[CH:12]=[CH:13][C:14]([NH:17][S:18]([CH3:21])(=[O:19])=[O:20])=[CH:15][CH:16]=2)=[CH:7][CH:8]=1Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
Hydrogenate N-(4-fluorophenyl)-4-[(methylsulfonyl)amino]-N-[2-[(2-phenylethyl)(phenylmethyl)amino]ethyl]benzamide hydrochloride over palladium on carbon in ethanol at 30-40 psi. Follow the progress of the reaction by thinlayer chromatography on silica gel. At the completion of the reaction remove the catalyst by filtration and evaporate the solvent in vacuo to obtain the title compound.
Workup
- customthe progress of the reaction by thinlayer chromatography on silica gel
- customAt the completion of the reaction remove the catalyst
- filtrationby filtration
- customevaporate the solvent in vacuo
Sources & evidence
- ORD record
- ord-3bfc42208e98411c9c1ff6dfbd513b9e
- Source dataset
- uspto-grants-1990_04
- Patent number
- US04920116
Reaction notes
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