1-Piperonylpiperazine → HCID 14303514, compound

HRID 1723178Notes

Reaction equation

HRID 1723178 reaction equation
[F:1][C:2]1[CH:3]=[CH:4][C:5]2[O:9][C:8](=[O:10])[C:7]([CH2:17][C:18]([Cl:20])=[O:19])([C:11]3[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=3)[C:6]=2[CH:21]=1.[CH2:22]1[O:37][C:36]2[CH:35]=[CH:34][C:26]([CH2:27][N:28]3[CH2:33][CH2:32][NH:31][CH2:30][CH2:29]3)=[CH:25][C:24]=2[O:23]1>>[ClH:20].[F:1][C:2]1[CH:3]=[CH:4][C:5]2[O:9][C:8](=[O:10])[C:7]([CH2:17][C:18]([N:31]3[CH2:32][CH2:33][N:28]([CH2:27][C:26]4[CH:34]=[CH:35][C:36]5[O:37][CH2:22][O:23][C:24]=5[CH:25]=4)[CH2:29][CH2:30]3)=[O:19])([C:11]3[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=3)[C:6]=2[CH:21]=1

Participants

3

Reactant 2

HCID 944261-PiperonylpiperazineHCID 19838005HCID 19838005, compound

Product 1

HCID 14303514HCID 14303514, compound

Procedure

This compound was prepared according to the process described in Example 9, starting with 2-(5-fluoro-2,3-dihydro-2-oxo-3-phenyl-3-benzofuranyl)acetyl chloride and 4-(3,4-methyenedioxybenzyl)piperazine.

Workup

  1. customThis compound was prepared

Sources & evidence

ORD record
ord-9b754378926b4d6ebfb77dee1861621b
Source dataset
uspto-grants-1989_08
Patent number
US04859700

Reaction notes

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