HCID 59335099, compound → HCID 59335142, compound
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([S:10]([N:13]([CH2:29][C:30]([OH:32])=[O:31])[C:14]2[CH:15]=[CH:16][C:17]3[N:18]([CH2:27][CH3:28])[C:19]4[C:24]([C:25]=3[CH:26]=2)=[CH:23][CH:22]=[CH:21][CH:20]=4)(=[O:12])=[O:11])[CH:5]=[C:6]([C:8]#[CH:9])[CH:7]=1.[H][H]>C(OCC)(=O)C.[Pt](=O)=O>[Cl:1][C:2]1[CH:3]=[C:4]([S:10]([N:13]([CH2:29][C:30]([OH:32])=[O:31])[C:14]2[CH:15]=[CH:16][C:17]3[N:18]([CH2:27][CH3:28])[C:19]4[C:24]([C:25]=3[CH:26]=2)=[CH:23][CH:22]=[CH:21][CH:20]=4)(=[O:12])=[O:11])[CH:5]=[C:6]([CH2:8][CH3:9])[CH:7]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
104 mg [(3-chloro-5-ethynyl-phenylsulphonyl)-(9-ethyl-9H-carbazol-3-yl)-amino]-acetic acid are dissolved in 5 ml of ethyl acetate. 30 mg of platinum dioxide are added and the mixture is hydrogenated for 5.5 hours at 3 bar hydrogen pressure. Then the catalyst is removed by suction filtering, the solvent is eliminated in vacuo and the residue is purified by preparative HPLC.
Workup
- customThen the catalyst is removed by suction
- filtrationfiltering
- customthe residue is purified by preparative HPLC
Sources & evidence
- ORD record
- ord-ae06f466f7b84fecafc415cb64af8e22
- Source dataset
- uspto-grants-2012_07
- Patent number
- US08232312B2
Reaction notes
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