(2,5-Dichloro-phenyl)-piperidin-4-yl-methanone → HCID 178453903, compound

HRID 1961649Notes

Reaction equation

HRID 1961649 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([Cl:8])=[CH:4][C:3]=1[C:9]([CH:11]1[CH2:16][CH2:15][NH:14][CH2:13][CH2:12]1)=[O:10].[C:17]([O:21][C:22](=[O:33])[NH:23][C@H:24]1[CH2:29][CH2:28][C@H:27]([CH2:30][CH:31]=O)[CH2:26][CH2:25]1)([CH3:20])([CH3:19])[CH3:18]>>[C:17]([O:21][C:22](=[O:33])[NH:23][C@H:24]1[CH2:25][CH2:26][C@H:27]([CH2:30][CH2:31][N:14]2[CH2:13][CH2:12][CH:11]([C:9](=[O:10])[C:3]3[CH:4]=[C:5]([Cl:8])[CH:6]=[CH:7][C:2]=3[Cl:1])[CH2:16][CH2:15]2)[CH2:28][CH2:29]1)([CH3:20])([CH3:19])[CH3:18]

Participants

3

Reactant 2

HCID 43344621(2,5-Dichloro-phenyl)-piperidin-4-yl-methanoneHCID 178453924HCID 178453924, compound

Product 1

HCID 178453903HCID 178453903, compound

Procedure

The title compound was prepared as described on example 1 from (2,5-Dichloro-phenyl)-piperidin-4-yl-methanone and Trans-[4-(2-Oxo-ethyl)-cyclohexyl]-carbamic acid tert-butyl ester (m/e): 483.5 (M+H+)

Sources & evidence

ORD record
ord-965d2c8f5ec7447394b5963ebc20feea
Source dataset
uspto-grants-2013_04
Patent number
US08415350B2

Reaction notes

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