Methyl 4-[2-fluoro-3-(methylsulfonyl)phenyl]piperazine-1-carboxylate → 1-[2-Fluoro-3-(methylsulfonyl)phenyl]piperazine
Reaction equation
[F:1][C:2]1[C:7]([S:8]([CH3:11])(=[O:10])=[O:9])=[CH:6][CH:5]=[CH:4][C:3]=1[N:12]1[CH2:17][CH2:16][N:15](C(OC)=O)[CH2:14][CH2:13]1>C(O)C.Cl>[F:1][C:2]1[C:7]([S:8]([CH3:11])(=[O:9])=[O:10])=[CH:6][CH:5]=[CH:4][C:3]=1[N:12]1[CH2:17][CH2:16][NH:15][CH2:14][CH2:13]1Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
Preparation according to preparation 29: methyl 4-[2-fluoro-3-(methylsulfonyl)phenyl]piperazine-1-carboxylate (1.0 g, 3.16 mmol) in ethanol (8 ml), hydrochloric acid (6 M, 20 ml). Yield: 0.34 g. MS m/z (rel. intensity, 70 eV) 258 (M+, 17), 215 (13), 216 (bp), 209 (6), 137 (9).
Workup
- customPreparation
- customaccording to preparation 29
Sources & evidence
- ORD record
- ord-a6abfe621f134602b5e87e19e7a5fb1d
- Source dataset
- uspto-grants-2010_07
- Patent number
- US07763639B2
Reaction notes
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