Acetic Acid → HCID 53248667, compound
Reaction equation
Cl[C:2]1[N:7]=[N:6][C:5]([C:8]2[C:9]3[N:10]([N:16]=[C:17]([CH:19]([CH3:21])[CH3:20])[CH:18]=3)[C:11]([O:14][CH3:15])=[CH:12][CH:13]=2)=[CH:4][CH:3]=1.C(O)(=[O:24])C>>[CH3:15][O:14][C:11]1[N:10]2[N:16]=[C:17]([CH:19]([CH3:21])[CH3:20])[CH:18]=[C:9]2[C:8]([C:5]2[CH:4]=[CH:3][C:2](=[O:24])[NH:7][N:6]=2)=[CH:13][CH:12]=1Participants
3
Conditions
- Temperature
- 90 °C
Procedure
The compound of Example 268 (50 mg) was dissolved in acetic acid (2 mL) and the solution was stirred at 90° C. for 3 hours. Subsequently, the solvent was concentrated and the residue was purified by silica gel column chromatography (methanol:ethyl acetate 1:9) to afford the title compound as a pale yellow powder (26 mg).
Workup
- concentrationSubsequently, the solvent was concentrated
- customthe residue was purified by silica gel column chromatography (methanol:ethyl acetate 1:9)
Sources & evidence
- ORD record
- ord-46fcf51da4d94b25b2cf06b0f9d50fec
- Source dataset
- uspto-grants-2010_07
- Patent number
- US07763617B2
Reaction notes
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