1-[3-(Dimethylamino)propyl]piperazine → HCID 69642243, compound

HRID 1794179Notes

Reaction equation

HRID 1794179 reaction equation
[CH3:1][N:2]([CH3:12])[CH2:3][CH2:4][CH2:5][N:6]1[CH2:11][CH2:10][NH:9][CH2:8][CH2:7]1.[ClH:13].[CH3:14][O:15][C:16]1[C:24]2[O:23][C:22]([CH3:26])([CH3:25])[CH2:21][C:20]=2[C:19]([C:27]2[C@@H:36]3[C@@H:31]([CH2:32][CH:33]=[CH:34][CH2:35]3)[C:30](=[O:37])[N:29]([C:38]3[CH:43]=[CH:42][C:41]([C:44](N4CCN(C/C=C/C5C=CC=CC=5)CC4)=[O:45])=[CH:40][CH:39]=3)[N:28]=2)=[CH:18][CH:17]=1>>[ClH:13].[ClH:13].[CH3:12][N:2]([CH3:1])[CH2:3][CH2:4][CH2:5][N:6]1[CH2:7][CH2:8][N:9]([C:44]([C:41]2[CH:42]=[CH:43][C:38]([N:29]3[N:28]=[C:27]([C:19]4[C:20]5[CH2:21][C:22]([CH3:26])([CH3:25])[O:23][C:24]=5[C:16]([O:15][CH3:14])=[CH:17][CH:18]=4)[C@@H:36]4[C@@H:31]([CH2:32][CH:33]=[CH:34][CH2:35]4)[C:30]3=[O:37])=[CH:39][CH:40]=2)=[O:45])[CH2:10][CH2:11]1

Participants

3

Reactant 2

HCID 27362341-[3-(Dimethylamino)propyl]piperazineHCID 69642098HCID 69642098, compound

Product 1

HCID 69642243HCID 69642243, compound

Procedure

Prepared from intermediate product A2 and 1-(3-dimethylaminopropyl)-piperazine as described for compound 8. M.p. 262° C. (with decomposition).

Sources & evidence

ORD record
ord-8de8d2beeb474ddeadd2eb430fb3937f
Source dataset
uspto-grants-2006_04
Patent number
US07022696B2

Reaction notes

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