(1,1-Dimethyl-prop-2-ynyl)-ethyl-(2-methoxy-ethyl)-amine → {1,1-Dimethyl-3-[3-(4-trifluoromethyl-phenyl)-benzo[d]isothiazol-6-yl]-prop-2-ynyl}-ethyl-(2-methoxy-ethyl)-amine
Reaction equation
[F:1][C:2]([F:27])([F:26])[C:3]1[CH:8]=[CH:7][C:6]([C:9]2[C:13]3[CH:14]=[CH:15][C:16](OS(C(F)(F)F)(=O)=O)=[CH:17][C:12]=3[S:11][N:10]=2)=[CH:5][CH:4]=1.[CH3:28][C:29]([N:33]([CH2:38][CH3:39])[CH2:34][CH2:35][O:36][CH3:37])([CH3:32])[C:30]#[CH:31]>>[CH3:32][C:29]([N:33]([CH2:38][CH3:39])[CH2:34][CH2:35][O:36][CH3:37])([CH3:28])[C:30]#[C:31][C:16]1[CH:15]=[CH:14][C:13]2[C:9]([C:6]3[CH:5]=[CH:4][C:3]([C:2]([F:26])([F:27])[F:1])=[CH:8][CH:7]=3)=[N:10][S:11][C:12]=2[CH:17]=1Participants
3
Reactant 2
Product 1
Procedure
In analogy to example 14.1, Trifluoro-methanesulfonic acid 3-(4-trifluoromethyl-phenyl)-benzo[d]isothiazol-6-yl ester and (1,1-Dimethyl-prop-2-ynyl)-ethyl-(2-methoxy-ethyl)-amine were converted to yield {1,1-Dimethyl-3-[3-(4-trifluoromethyl-phenyl)-benzo[d]isothiazol-6-yl]-prop-2-ynyl}-ethyl-(2-methoxy-ethyl)-amine as brown oil, MS: 447 (MH+).
Sources & evidence
- ORD record
- ord-3bc6d7049271416cac5c232fa9ff741e
- Source dataset
- uspto-grants-2008_11
- Patent number
- US07449483B2
Reaction notes
Loading…