3,4-Difluorobenzene-1-sulfonyl chloride → (S)-Methyl 2-(6-(4-(3,4-difluorophenylsulfonamido)phenyl)-1-oxoisoindolin-2-yl)-3-methylbutanoate
Reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:16]=[C:15]3[C:11]([CH2:12][N:13]([C@@H:18]([CH:23]([CH3:25])[CH3:24])[C:19]([O:21][CH3:22])=[O:20])[C:14]3=[O:17])=[CH:10][CH:9]=2)=[CH:4][CH:3]=1.[F:26][C:27]1[CH:28]=[C:29]([S:34](Cl)(=[O:36])=[O:35])[CH:30]=[CH:31][C:32]=1[F:33]>>[F:26][C:27]1[CH:28]=[C:29]([S:34]([NH:1][C:2]2[CH:3]=[CH:4][C:5]([C:8]3[CH:16]=[C:15]4[C:11]([CH2:12][N:13]([C@@H:18]([CH:23]([CH3:25])[CH3:24])[C:19]([O:21][CH3:22])=[O:20])[C:14]4=[O:17])=[CH:10][CH:9]=3)=[CH:6][CH:7]=2)(=[O:35])=[O:36])[CH:30]=[CH:31][C:32]=1[F:33]Participants
3
Procedure
The compound of example 81 was prepared analogous to compound of example 77 by reaction of compound of example 6 with 3,4-difluorobenzene sulfonyl chloride. The compound of example 81 was used directly without isolation for the preparation of compound of example 82.
Sources & evidence
- ORD record
- ord-e3e1a44237f44f12bb89ccc750cabea6
- Source dataset
- uspto-grants-2014_06
- Patent number
- US08748426B2
Reaction notes
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