Methyl iodide → {(R)-4-[(3-methanesulfonyl-5-trifluoromethyl-benzene-sulfonyl)-methyl-amino]-4,5,6,7-tetrahydro-indazol-1-yl}-acetic acid ethyl ester
Reaction equation
[CH2:1]([O:3][C:4](=[O:33])[CH2:5][N:6]1[C:14]2[CH2:13][CH2:12][CH2:11][C@@H:10]([NH:15][S:16]([C:19]3[CH:24]=[C:23]([C:25]([F:28])([F:27])[F:26])[CH:22]=[C:21]([S:29]([CH3:32])(=[O:31])=[O:30])[CH:20]=3)(=[O:18])=[O:17])[C:9]=2[CH:8]=[N:7]1)[CH3:2].[CH3:34]I>>[CH2:1]([O:3][C:4](=[O:33])[CH2:5][N:6]1[C:14]2[CH2:13][CH2:12][CH2:11][C@@H:10]([N:15]([S:16]([C:19]3[CH:24]=[C:23]([C:25]([F:27])([F:26])[F:28])[CH:22]=[C:21]([S:29]([CH3:32])(=[O:30])=[O:31])[CH:20]=3)(=[O:17])=[O:18])[CH3:34])[C:9]=2[CH:8]=[N:7]1)[CH3:2]Participants
3
Reactant 2
Product 1
Procedure
Starting with [(R)-4-(3-methanesulfonyl-5-trifluoromethyl-benzenesulfonylamino)-4,5,6,7-tetrahydro-indazol-1-yl]-acetic acid ethyl ester (example 5-1) and methyl iodide using the method analogous to the one described for example 2-1, {(R)-4-[(3-methanesulfonyl-5-trifluoromethyl-benzene-sulfonyl)-methyl-amino]-4,5,6,7-tetrahydro-indazol-1-yl}-acetic acid ethyl ester was obtained MS cald. for C20H24F3N3O6S2 523, obsd. (ESI+) [(M+H)+]: 524.
Sources & evidence
- ORD record
- ord-0d379f437afa401ca5b2ffbd16d2b3a0
- Source dataset
- uspto-grants-2012_09
- Patent number
- US08268870B2
Reaction notes
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