Acetic Anhydride → HCID 22284133, compound
Reaction equation
[C:1]([O:4][C:5](=O)[CH3:6])(=[O:3])[CH3:2].[C:8]([N:11]1[CH:16]=[C:15]([C:17]2[CH:22]=[C:21]([OH:23])[C:20]([OH:24])=C(O)C=2)[N:14]([CH2:26][C:27]([OH:29])=[O:28])[C:13](=[O:30])[CH:12]1[CH:31]([CH3:33])[CH3:32])(=[O:10])[CH3:9]>CC(C)=O>[C:8]([N:11]1[CH:16]=[C:15]([C:17]2[CH:6]=[C:5]([O:4][C:1](=[O:3])[CH3:2])[C:20]([O:24][C:1](=[O:3])[CH3:2])=[C:21]([O:23][C:5](=[O:4])[CH3:6])[CH:22]=2)[N:14]([CH2:26][C:27]([OH:29])=[O:28])[C:13](=[O:30])[CH:12]1[CH:31]([CH3:33])[CH3:32])(=[O:10])[CH3:9]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Acetic anhydride is added to a suspension of {(3RS)-4-acetyl-3-isopropyl-2-oxo-6-(3,4,5-trihydroxyphenyl)-1,2,3,4-tetrahydropyrazin-1-yl}acetic acid (630 mg, Reference compound No. 62-2) in acetone (10 ml), and the mixture is stirred for one week. The reaction mixture is concentrated under reduced pressure to give the titled reference compound (790 mg).
Workup
- concentrationThe reaction mixture is concentrated under reduced pressure
Sources & evidence
- ORD record
- ord-c3734e76eb324bb6b149e7e645a6c57e
- Source dataset
- uspto-grants-2005_11
- Patent number
- US06960575B2
Reaction notes
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