Trifluoroacetic acid → HCID 86591704, compound
Reaction equation
[C:1]([CH:3]=[C:4]1[CH2:9][CH2:8][N:7]([C:10]2[CH:15]=[CH:14][C:13]([N:16]3[CH2:20][C@H:19]([CH2:21][NH2:22])[O:18][C:17]3=[O:23])=[CH:12][C:11]=2[F:24])[CH2:6][CH:5]1[CH3:25])#[N:2].[F:26][C:27]([F:32])([F:31])[C:28](O)=[O:29]>>[C:1]([CH:3]=[C:4]1[CH2:9][CH2:8][N:7]([C:10]2[CH:15]=[CH:14][C:13]([N:16]3[CH2:20][C@H:19]([CH2:21][NH:22][C:28](=[O:29])[C:27]([F:32])([F:31])[F:26])[O:18][C:17]3=[O:23])=[CH:12][C:11]=2[F:24])[CH2:6][CH:5]1[CH3:25])#[N:2]Participants
3
Procedure
The title compound was prepared as per Example-29 by using (S)-N-{3-[4-(4-cyanomethylidene-3-methylpiperidin-1-yl)-3-fluorophenyl]-2-oxo-oxazolidin-5-ylmethyl}-amine and trifluoroacetic acid in 51% yield.
Sources & evidence
- ORD record
- ord-e6976f12c6144ab78030679bed107dad
- Source dataset
- uspto-grants-2008_07
- Patent number
- US07405228B2
Reaction notes
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