Dimethylamine → HCID 68806601, compound
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.[CH3:26][NH:27][CH3:28]>>[ClH:1].[ClH:1].[CH:21]1([N:18]2[CH2:19][CH2:20][CH:15]([CH2:14][C:11]3[N:10]=[C:9]([C:6]4[CH:7]=[CH:8][C:3]([CH2:2][N:27]([CH3:28])[CH3:26])=[CH:4][CH:5]=4)[O:13][N:12]=3)[CH2:16][CH2:17]2)[CH2:25][CH2:24][CH2:23][CH2:22]1Participants
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-cyclopentylpiperidine and dimethylamine. HPLC: Rt=4.43 min.
Sources & evidence
- ORD record
- ord-74bc16d66e2e4532b9f112c462140a70
- Source dataset
- uspto-grants-2010_09
- Patent number
- US07799924B2
Reaction notes
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