Trifluoroacetic acid → HCID 22224850, compound
Reaction equation
[O:1]=[C:2]([C:7]1[CH:12]=[CH:11][N:10]=[CH:9][CH:8]=1)[CH2:3][C:4]([OH:6])=[O:5].[C:13](O)([C:15](F)(F)F)=O.[C:20](OC(C(F)(F)F)=O)(C(F)(F)F)=O>CC(C)=O>[CH3:20][C:13]1([CH3:15])[O:5][C:4](=[O:6])[CH:3]=[C:2]([C:7]2[CH:12]=[CH:11][N:10]=[CH:9][CH:8]=2)[O:1]1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Prepared from 3-oxo-3-pyridin-4-yl-propionic acid [prepared from 4-acetylpyridine, magnesium methylcarbonate and CO2 in DMF at 120° C. according to Journal of Antibiotics 1978, 31, 1245] by treatment with acetone, TFA and TFAA according to general procedure J (method b). Obtained as a white solid (1.3 g).
Sources & evidence
- ORD record
- ord-d01fe35baedb44628fc604ddde5af179
- Source dataset
- uspto-grants-2006_03
- Patent number
- US07018998B2
Reaction notes
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