2-Methylpiperazine, (S)- → 2-Methyl-5-[(3S)-3-methyl-1-piperazinyl]quinoline
Reaction equation
[CH3:1][C@H:2]1[CH2:7][NH:6][CH2:5][CH2:4][NH:3]1.FC(F)(F)S(O[C:14]1[CH:23]=[CH:22][CH:21]=[C:20]2[C:15]=1[CH:16]=[CH:17][C:18]([CH3:24])=[N:19]2)(=O)=O>>[CH3:24][C:18]1[CH:17]=[CH:16][C:15]2[C:20](=[CH:21][CH:22]=[CH:23][C:14]=2[N:6]2[CH2:5][CH2:4][NH:3][C@@H:2]([CH3:1])[CH2:7]2)[N:19]=1Participants
3
Procedure
The title compound was prepared in 27% yield using a similar procedure to Example 127 starting from (2S)-2-methylpiperazine and 2-methyl-5-quinolinyl trifluoromethanesulfonate (D1).
Sources & evidence
- ORD record
- ord-d3aacf1c3f59428896e0936f8e082cdc
- Source dataset
- uspto-grants-2009_09
- Patent number
- US07592346B2
Reaction notes
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