2-(Methylamino)ethanol → 2-[[2-[3-(4-Bromo-phenyl)-benzo[d]isothiazol-6-yloxy]-ethyl]-methyl-amino]-ethanol
Reaction equation
Br[CH2:2][CH2:3][O:4][C:5]1[CH:20]=[CH:19][C:8]2[C:9]([C:12]3[CH:17]=[CH:16][C:15]([Br:18])=[CH:14][CH:13]=3)=[N:10][S:11][C:7]=2[CH:6]=1.[CH3:21][NH:22][CH2:23][CH2:24][OH:25]>>[Br:18][C:15]1[CH:16]=[CH:17][C:12]([C:9]2[C:8]3[CH:19]=[CH:20][C:5]([O:4][CH2:3][CH2:2][N:22]([CH3:21])[CH2:23][CH2:24][OH:25])=[CH:6][C:7]=3[S:11][N:10]=2)=[CH:13][CH:14]=1Participants
3
Procedure
According to the method in example 4, 6-(2-Bromo-ethoxy)-3-(4-bromo-phenyl)-benzo[d]isothiazole and 2-(methylamino)ethanol were converted to yield 2-[[2-[3-(4-Bromo-phenyl)-benzo[d]isothiazol-6-yloxy]-ethyl]-methyl-amino]-ethanol, MS: 408 (MH+, 1Br).
Sources & evidence
- ORD record
- ord-2856407f60d9423da3926cc1d3d6fe1d
- Source dataset
- uspto-grants-2007_02
- Patent number
- US07173043B2
Reaction notes
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