Loxoprofen Impurity 18 → HCID 66913788, compound
Reaction equation
[Cl:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:11]=1[N:10]=[CH:9][C:8]([CH3:12])=[C:7]2[C:13]1[CH:14]=[C:15]([OH:19])[CH:16]=[CH:17][CH:18]=1.C[O:21][C:22](=[O:33])[CH:23]([C:25]1[CH:30]=[CH:29][C:28]([CH2:31]Br)=[CH:27][CH:26]=1)[CH3:24]>>[Cl:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:11]=1[N:10]=[CH:9][C:8]([CH3:12])=[C:7]2[C:13]1[CH:14]=[C:15]([CH:16]=[CH:17][CH:18]=1)[O:19][CH2:31][C:28]1[CH:27]=[CH:26][C:25]([C@@H:23]([CH3:24])[C:22]([OH:33])=[O:21])=[CH:30][CH:29]=1Participants
3
Procedure
This compound was prepared according to the procedure of example 41, substituting 3-(8-chloro-3-methyl-quinolin-4-yl)-phenol and 2-(4-bromomethyl-phenyl)-propionic acid methyl ester. Purification by supercritical fluid chromatography (MeOH/CO2). Electronic circular dichroism CD λmax=+6 mdeg @ 226 nm (EtOH). MS (ESI) m/z 432.
Workup
- customThis compound was prepared
- customPurification by supercritical fluid chromatography (MeOH/CO2)
Sources & evidence
- ORD record
- ord-29b5d020b4f84b39887ed37dbc9126a6
- Source dataset
- uspto-grants-2009_08
- Patent number
- US07576215B2
Reaction notes
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