1-Phenylpiperazine → HCID 59657793, compound

HRID 1715760Notes

Reaction equation

HRID 1715760 reaction equation
Cl[CH2:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[O:13][N:12]=[C:11]([CH2:14][CH:15]3[CH2:20][CH2:19][N:18]([CH:21]4[CH2:25][CH2:24][CH2:23][CH2:22]4)[CH2:17][CH2:16]3)[N:10]=2)=[CH:5][CH:4]=1.[C:26]1([N:32]2[CH2:37][CH2:36][NH:35][CH2:34][CH2:33]2)[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1>>[CH:21]1([N:18]2[CH2:17][CH2:16][CH:15]([CH2:14][C:11]3[N:10]=[C:9]([C:6]4[CH:7]=[CH:8][C:3]([CH2:2][N:35]5[CH2:36][CH2:37][N:32]([C:26]6[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=6)[CH2:33][CH2:34]5)=[CH:4][CH:5]=4)[O:13][N:12]=3)[CH2:20][CH2:19]2)[CH2:22][CH2:23][CH2:24][CH2:25]1

Participants

3

Procedure

The title compound was prepared by a similar procedure to that described in Example 23, starting from 4-[5-(4-chloromethylphenyl) [1,2,4]oxadiazol-3-ylmethyl]-1-cyclopentyl-piperidine and 1-phenylpiperazine.

Sources & evidence

ORD record
ord-372bc5b362c4462e95397089ba7d3d2f
Source dataset
uspto-grants-2010_09
Patent number
US07799924B2

Reaction notes

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