2,3-Dihydroxybutanedioic Acid → HCID 66933855, compound
Reaction equation
[C:1]([OH:10])(=[O:9])[CH:2]([CH:4]([C:6]([OH:8])=[O:7])[OH:5])[OH:3].[Cl:11][C:12]1[CH:17]=[C:16]([Cl:18])[C:15]([F:19])=[CH:14][C:13]=1[C:20]1[O:21][C:22]2[C:27]([C:28](=[O:30])[CH:29]=1)=[C:26]([OH:31])[CH:25]=[C:24]([OH:32])[C:23]=2[C@@H:33]1[CH2:37][CH2:36][N:35]([CH3:38])[C@H:34]1[CH2:39][OH:40]>CO>[C:6]([CH:4]([CH:2]([C:1]([OH:10])=[O:9])[OH:3])[OH:5])([OH:8])=[O:7].[Cl:11][C:12]1[CH:17]=[C:16]([Cl:18])[C:15]([F:19])=[CH:14][C:13]=1[C:20]1[O:21][C:22]2[C:27]([C:28](=[O:30])[CH:29]=1)=[C:26]([OH:31])[CH:25]=[C:24]([OH:32])[C:23]=2[C@@H:33]1[CH2:37][CH2:36][N:35]([CH3:38])[C@H:34]1[CH2:39][OH:40]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 52.5 °C
Procedure
Tartaric acid (0.016 g, 0.11 mmol) was added to the suspension of compound of example 47 (0.05 g, 0.11 mmol) in methanol (2 mL). It was stirred for 10 min. at 50-55° C. The reaction mixture was concentrated and solid was dried to obtain the title compound.
Workup
- concentrationThe reaction mixture was concentrated
- customsolid was dried
Sources & evidence
- ORD record
- ord-abe2ab1dbce84994b814e94b28728657
- Source dataset
- uspto-grants-2011_02
- Patent number
- US07884127B2
Reaction notes
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