HCID 68842200, compound → HCID 57777470, compound
Reaction equation
C([O:8][C:9]1[CH:10]=[C:11]([CH:21]=[CH:22][C:23]=1[N:24]1[CH2:28][C:27](=[O:29])[NH:26][S:25]1(=[O:31])=[O:30])[CH2:12][C:13]1[CH:20]=[CH:19][CH:18]=[CH:17][C:14]=1[C:15]#[N:16])C1C=CC=CC=1>CCO.O.[Pd]>[NH2:16][CH2:15][C:14]1[CH:17]=[CH:18][CH:19]=[CH:20][C:13]=1[CH2:12][C:11]1[CH:21]=[CH:22][C:23]([N:24]2[S:25](=[O:31])(=[O:30])[NH:26][C:27](=[O:29])[CH2:28]2)=[C:9]([OH:8])[CH:10]=1Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
A solution of 2-[3-benzyloxy-4-(1,1,4-trioxo-1,2,5-thiadiazolidin-2-yl)-benzyl]-benzonitrile in EtOH/water (1:1) is hydrogenated at 1 atm over 10% Pd/C for 40 min. The catalyst is filtered, the solvent evaporated and the residue purified by preparative HPLC to give the title compound.
Workup
- filtrationThe catalyst is filtered
- customthe solvent evaporated
- customthe residue purified by preparative HPLC
Sources & evidence
- ORD record
- ord-db52030bf3ee440296d30a80d4a44909
- Source dataset
- uspto-grants-2011_12
- Patent number
- US08084448B2
Reaction notes
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