1-(3-Aminopropyl)-4-methylpiperazine → HCID 91335553, compound
Reaction equation
[CH3:1][N:2]1[CH2:7][CH2:6][N:5]([CH2:8][CH2:9][CH2:10][NH2:11])[CH2:4][CH2:3]1.[Cl:12][C:13]1[CH:18]=[CH:17][N:16]=[C:15]2[CH:19]=[C:20]([C:22]([O-])=[O:23])[S:21][C:14]=12.[Li+]>>[CH3:1][N:2]1[CH2:7][CH2:6][N:5]([CH2:8][CH2:9][CH2:10][NH:11][C:22]([C:20]2[S:21][C:14]3[C:15](=[N:16][CH:17]=[CH:18][C:13]=3[Cl:12])[CH:19]=2)=[O:23])[CH2:4][CH2:3]1Participants
3
Procedure
The title compound was prepared from 3-(4-methylpiperazin-1-yl)-propylamine and lithium 7-chloro-thieno[3,2-b]pyridine-2-carboxylate by a procedure analogous to Example 1B. MS: 353/355 (MH+); HPLC Rf: n.d.; HPLC purity: n.d.
Sources & evidence
- ORD record
- ord-7af260d248f146dba188c008208ee7f5
- Source dataset
- uspto-grants-2005_11
- Patent number
- US06964961B2
Reaction notes
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