1-Methylpiperazine → HCID 20553457, compound
Reaction equation
Cl.Cl[CH2:3][CH2:4][CH2:5][O:6][C:7]1[CH:8]=[CH:9][C:10]2[C:19]([CH:20]=1)=[N:18][C:17]1[C:12](=[CH:13][CH:14]=[C:15]([O:21][CH2:22][CH2:23][CH2:24]Cl)[CH:16]=1)[CH:11]=2.[CH3:26][N:27]1[CH2:32][CH2:31][NH:30][CH2:29][CH2:28]1>>[CH3:26][N:27]1[CH2:32][CH2:31][N:30]([CH2:3][CH2:4][CH2:5][O:6][C:7]2[CH:8]=[CH:9][C:10]3[C:19]([CH:20]=2)=[N:18][C:17]2[C:12](=[CH:13][CH:14]=[C:15]([O:21][CH2:22][CH2:23][CH2:24][N:30]4[CH2:31][CH2:32][N:27]([CH3:26])[CH2:28][CH2:29]4)[CH:16]=2)[CH:11]=3)[CH2:29][CH2:28]1Participants
3
Procedure
The compound is prepared from 3,6-bis(3-chloropropoxy)acridine hydrochloride and N-methylpiperazine as described in Example 44.
Sources & evidence
- ORD record
- ord-8ca946307eae4519ae663cafccc59a87
- Source dataset
- uspto-grants-1982_02
- Patent number
- US04314061
Reaction notes
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