N-Methylisopropylamine → HCID 69287930, compound
Reaction equation
Br[CH2:2][CH2:3][CH2:4][CH2:5][O:6][C:7]1[CH:22]=[CH:21][C:10]2[C:11]([C:14]3[CH:19]=[CH:18][C:17]([Cl:20])=[CH:16][CH:15]=3)=[N:12][S:13][C:9]=2[CH:8]=1.[CH:23]([NH:26][CH3:27])([CH3:25])[CH3:24]>>[Cl:20][C:17]1[CH:18]=[CH:19][C:14]([C:11]2[C:10]3[CH:21]=[CH:22][C:7]([O:6][CH2:5][CH2:4][CH2:3][CH2:2][N:26]([CH:23]([CH3:25])[CH3:24])[CH3:27])=[CH:8][C:9]=3[S:13][N:12]=2)=[CH:15][CH:16]=1Participants
3
Procedure
According to the method in example 7, 6-(4-Bromo-butoxy)-3-(4-chloro-phenyl)-benzo[d]isothiazole and N-Isopropylmethylamine were converted to yield {4-[3-(4-Chloro-phenyl)-benzo[d]isothiazol-6-yloxy]-butyl}-isopropyl-methyl-amine, MS: 389 (MH+, 1Cl).
Sources & evidence
- ORD record
- ord-94c42b0abcc74fe0a276e095af422a9c
- Source dataset
- uspto-grants-2008_11
- Patent number
- US07449483B2
Reaction notes
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