3-(Trifluoromethoxy)benzene-1-sulfonyl chloride → 3-[3-(3-Trifluoromethoxy-benzenesulfonylamino)-phenyl]-pyrrolidine-1-carboxylic acid methyl ester
Reaction equation
[F:1][C:2]([F:29])([F:28])[O:3][C:4]1[CH:5]=[C:6]([S:10]([NH:13][C:14]2[CH:19]=[CH:18][C:17]([C@@H]3CCN(CCC)C3)=[CH:16][CH:15]=2)(=[O:12])=[O:11])[CH:7]=[CH:8][CH:9]=1.[CH3:30][O:31][C:32]([N:34]1[CH2:38][CH2:37][CH:36](C2C=CC=C(N)C=2)[CH2:35]1)=[O:33].FC(F)(F)OC1C=C(S(Cl)(=O)=O)C=CC=1>>[CH3:30][O:31][C:32]([N:34]1[CH2:38][CH2:37][CH:36]([C:16]2[CH:17]=[CH:18][CH:19]=[C:14]([NH:13][S:10]([C:6]3[CH:7]=[CH:8][CH:9]=[C:4]([O:3][C:2]([F:28])([F:1])[F:29])[CH:5]=3)(=[O:11])=[O:12])[CH:15]=2)[CH2:35]1)=[O:33]Participants
4
Reactant 3
Product 1
Procedure
This compound was obtained following the same synthetic procedure as described for 3-trifluoromethoxy-N-[4-((S)-1-propyl-pyrrolidin-3-yl)-phenyl]-benzenesulfonamide by reacting 1-(Methoxycarbonyl)-3-(3-aminophenyl)-pyrrolidine as obtained in example b.1 with commercially available 3-trifluoromethoxy-benzenesulfonyl chloride.
Workup
- customThis compound was obtained
Sources & evidence
- ORD record
- ord-6f8ffb0385e44fec978fc3fcfce11804
- Source dataset
- uspto-grants-2014_02
- Patent number
- US08642642B2
Reaction notes
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