2-Chloronicotinic acid → HCID 11530576, compound
Reaction equation
Cl[C:2]1[C:7]([C:8]([N:10]2[CH2:15][CH2:14][N:13]([CH:16]([CH3:18])[CH3:17])[CH2:12][CH2:11]2)=[O:9])=[CH:6][CH:5]=[CH:4][N:3]=1.Cl[C:20]1[N:28]=[CH:27][CH:26]=[CH:25][C:21]=1C(O)=O.[CH:29]([N:32]1CCNCC1)(C)[CH3:30]>>[CH:16]([N:13]1[CH2:14][CH2:15][N:10]([C:8]([C:7]2[C:2]([NH:32][CH2:29][CH2:30][N:28]3[CH2:20][CH2:21][CH2:25][CH2:26][CH2:27]3)=[N:3][CH:4]=[CH:5][CH:6]=2)=[O:9])[CH2:11][CH2:12]1)([CH3:18])[CH3:17]Participants
4
Procedure
(2-Chloro-pyridin-3-yl)-(4-isopropyl-piperazin-1-yl)-methanone. The title compound was prepared in a manner similar to that described in Step A of Example 9 using 2-chloro-nicotinic acid and 1-isopropyl-piperazine.
Sources & evidence
- ORD record
- ord-7297992fd01642f9a8bb871cd0f6f222
- Source dataset
- uspto-grants-2011_05
- Patent number
- US07947718B2
Reaction notes
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