Azetidine → N-[Azetidin-1-yl(methyl)oxo-lambda6-sulfanylidene]-4-bromoaniline
Reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([NH:8][S:9]([CH3:11])=[O:10])=[CH:4][CH:3]=1.[NH:12]1[CH2:15][CH2:14][CH2:13]1>>[N:12]1([S:9]([CH3:11])(=[O:10])=[N:8][C:5]2[CH:6]=[CH:7][C:2]([Br:1])=[CH:3][CH:4]=2)[CH2:15][CH2:14][CH2:13]1Participants
3
Procedure
The title compound is prepared from N-(4-bromophenyl)methanesulfinamide and azetidine following a procedure analogous to that described for Intermediate 3 (Step 2). LC (method 1): tR=0.92 min; Mass spectrum (ESI+): m/z=289, 291 [M+H]+.
Sources & evidence
- ORD record
- ord-9e7e44c468b54107971b1c5ebc84ba9a
- Source dataset
- uspto-grants-2016_08
- Patent number
- US09422312B2
Reaction notes
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