Succinic Acid → HCID 86754646, compound
Reaction equation
[C:1]([OH:8])(=[O:7])[CH2:2][CH2:3][C:4]([OH:6])=[O:5].[Cl:9][C:10]1[CH:15]=[CH:14][C:13]([N:16]2[CH2:20][CH2:19][C@H:18]([CH2:21][N:22]3[CH2:27][CH2:26][N:25]([CH2:28][CH2:29][O:30][CH3:31])[CH2:24][CH2:23]3)[C:17]2=[O:32])=[CH:12][CH:11]=1>C(O)C>[C:1]([OH:8])(=[O:7])[CH2:2][CH2:3][C:4]([OH:6])=[O:5].[C:1]([OH:8])(=[O:7])[CH2:2][CH2:3][C:4]([OH:6])=[O:5].[Cl:9][C:10]1[CH:15]=[CH:14][C:13]([N:16]2[CH2:20][CH2:19][C@H:18]([CH2:21][N:22]3[CH2:23][CH2:24][N:25]([CH2:28][CH2:29][O:30][CH3:31])[CH2:26][CH2:27]3)[C:17]2=[O:32])=[CH:12][CH:11]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 591 mg of succinic acid in 20 mL of ethanol was added to a solution of 880 mg of (R)-1-(4-chlorophenyl)-3-(4-(2-methoxyethyl)piperazin-1-yl)methyl-2-pyrrolidinone in 20 mL of ethanol. The mixture was stirred at room temperature and cooled. The precipitated solid was filtered and dried to give 356 mg of the title compound.
Workup
- temperaturecooled
- filtrationThe precipitated solid was filtered
- customdried
Sources & evidence
- ORD record
- ord-3bb06041a79a45b7a7de032453fec4c5
- Source dataset
- uspto-grants-1999_10
- Patent number
- US05969138
Reaction notes
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