Piperidine → HCID 68807285, compound

HRID 2055688Notes

Reaction equation

HRID 2055688 reaction equation
[Cl:1][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.[NH:26]1[CH2:31][CH2:30][CH2:29][CH2:28][CH2:27]1>>[ClH:1].[ClH:1].[N:26]1([CH2:2][C:3]2[CH:8]=[CH:7][C:6]([C:9]3[O:13][N:12]=[C:11]([CH2:14][CH:15]4[CH2:20][CH2:19][N:18]([CH:21]5[CH2:25][CH2:24][CH2:23][CH2:22]5)[CH2:17][CH2:16]4)[N:10]=3)=[CH:5][CH:4]=2)[CH2:31][CH2:30][CH2:29][CH2:28][CH2:27]1

Participants

3

Reactant 2

HCID 8082PiperidineHCID 68432098HCID 68432098, compound

Product 1

HCID 68807285HCID 68807285, compound

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-cyclopentylpiperidine and piperidine. HPLC: Rt=6.74 min.

Sources & evidence

ORD record
ord-121f02c4c02c461f8dc4cdc57d43199c
Source dataset
uspto-grants-2008_02
Patent number
US07332508B2

Reaction notes

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