1-[(3,4,5-Trimethoxyphenyl)methyl]piperazine → HCID 13772361, compound

HRID 1710115Notes

Reaction equation

HRID 1710115 reaction equation
Br[CH2:2][CH2:3][CH2:4][CH2:5][O:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=1[C:13]1([CH:24]([CH3:26])[CH3:25])[C:21]2[C:16](=[CH:17][CH:18]=[CH:19][CH:20]=2)[N:15]([CH3:22])[C:14]1=[O:23].[CH3:27][O:28][C:29]1[CH:30]=[C:31]([CH:39]=[C:40]([O:44][CH3:45])[C:41]=1[O:42][CH3:43])[CH2:32][N:33]1[CH2:38][CH2:37][NH:36][CH2:35][CH2:34]1>>[CH:24]([C:13]1([C:8]2[CH:9]=[CH:10][CH:11]=[CH:12][C:7]=2[O:6][CH2:5][CH2:4][CH2:3][CH2:2][N:36]2[CH2:35][CH2:34][N:33]([CH2:32][C:31]3[CH:39]=[C:40]([O:44][CH3:45])[C:41]([O:42][CH3:43])=[C:29]([O:28][CH3:27])[CH:30]=3)[CH2:38][CH2:37]2)[C:21]2[C:16](=[CH:17][CH:18]=[CH:19][CH:20]=2)[N:15]([CH3:22])[C:14]1=[O:23])([CH3:26])[CH3:25]

Participants

3

Procedure

Preparation in analogy to Example (3d) from 3-[2-(4-bromobutoxy) phenyl]-3-isopropyl-1-methylindolin-2-one and 3,4,5-trimethoxybenzylpiperazine. Melting point 235°-237° C.

Sources & evidence

ORD record
ord-3409ae40496a465e838aeb20b2ee86d2
Source dataset
uspto-grants-1990_08
Patent number
US04952598

Reaction notes

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