p-Anisoyl chloride → HCID 68807410, compound

HRID 2055672Notes

Reaction equation

HRID 2055672 reaction equation
[CH:1]1([N:6]2[CH2:11][CH2:10][CH:9]([CH2:12][CH2:13][CH2:14][C:15]([NH:17][OH:18])=[NH:16])[CH2:8][CH2:7]2)[CH2:5][CH2:4][CH2:3][CH2:2]1.[CH3:19][O:20][C:21]1[CH:29]=[CH:28][C:24]([C:25]([Cl:27])=O)=[CH:23][CH:22]=1>>[ClH:27].[CH:1]1([N:6]2[CH2:7][CH2:8][CH:9]([CH2:12][CH2:13][CH2:14][C:15]3[N:16]=[C:25]([C:24]4[CH:28]=[CH:29][C:21]([O:20][CH3:19])=[CH:22][CH:23]=4)[O:18][N:17]=3)[CH2:10][CH2:11]2)[CH2:2][CH2:3][CH2:4][CH2:5]1

Participants

3

Reactant 2

HCID 7477p-Anisoyl chlorideHCID 178510956HCID 178510956, compound

Product 1

HCID 68807410HCID 68807410, compound

Procedure

The title compound was prepared by a similar procedure to that described in Example 3, starting from 4-(1-cyclopentylpiperidin-4-yl)-N-hydroxybutyramidine and 4-methoxybenzoyl chloride.

Sources & evidence

ORD record
ord-fd02c8bda9d94c448e32ec996fe9d9df
Source dataset
uspto-grants-2008_02
Patent number
US07332508B2

Reaction notes

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