1-(2-(Dimethylamino)ethyl)piperazine → HCID 69643167, compound
Reaction equation
[CH3:1][N:2]([CH3:11])[CH2:3][CH2:4][N:5]1[CH2:10][CH2:9][NH:8][CH2:7][CH2:6]1.[ClH:12].[CH3:13][O:14][C:15]1[C:23]2[O:22][C:21]([CH3:25])([CH3:24])[CH2:20][C:19]=2[C:18]([C:26]2[C@@H:35]3[C@@H:30]([CH2:31][CH:32]=[CH:33][CH2:34]3)[C:29](=[O:36])[N:28]([C:37]3[CH:42]=[CH:41][C:40]([C:43](N4CCN(C/C=C/C5C=CC=CC=5)CC4)=[O:44])=[CH:39][CH:38]=3)[N:27]=2)=[CH:17][CH:16]=1>>[ClH:12].[ClH:12].[CH3:1][N:2]([CH3:11])[CH2:3][CH2:4][N:5]1[CH2:10][CH2:9][N:8]([C:43]([C:40]2[CH:41]=[CH:42][C:37]([N:28]3[N:27]=[C:26]([C:18]4[C:19]5[CH2:20][C:21]([CH3:25])([CH3:24])[O:22][C:23]=5[C:15]([O:14][CH3:13])=[CH:16][CH:17]=4)[C@@H:35]4[C@@H:30]([CH2:31][CH:32]=[CH:33][CH2:34]4)[C:29]3=[O:36])=[CH:38][CH:39]=2)=[O:44])[CH2:7][CH2:6]1Participants
3
Procedure
Prepared from intermediate product A2 and 1-(2-dimethylaminoethyl)-piperazine as described for compound 8. M.p. 245° C. (with decomposition).
Sources & evidence
- ORD record
- ord-41dc6ca5f96744cfa3b2dfecaea61bfd
- Source dataset
- uspto-grants-2006_04
- Patent number
- US07022696B2
Reaction notes
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