4-Phenylbenzoyl chloride → HCID 131726776, compound

HRID 1715749Notes

Reaction equation

HRID 1715749 reaction equation
[CH2:1]([CH:3]([N:6]1[CH2:11][CH2:10][CH:9]([CH2:12][C:13]([NH:15][OH:16])=[NH:14])[CH2:8][CH2:7]1)[CH2:4][CH3:5])[CH3:2].[C:17]1([C:23]2[CH:31]=[CH:30][C:26]([C:27]([Cl:29])=O)=[CH:25][CH:24]=2)[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1>>[ClH:29].[CH2:1]([CH:3]([N:6]1[CH2:11][CH2:10][CH:9]([CH2:12][C:13]2[N:14]=[C:27]([C:26]3[CH:30]=[CH:31][C:23]([C:17]4[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=4)=[CH:24][CH:25]=3)[O:16][N:15]=2)[CH2:8][CH2:7]1)[CH2:4][CH3:5])[CH3:2]

Participants

3

Reactant 2

HCID 841514-Phenylbenzoyl chlorideHCID 178446096HCID 178446096, compound

Product 1

HCID 131726776HCID 131726776, compound

Procedure

The title compound was prepared by a similar procedure to that described in Example 12, starting from 2-((1-ethylpropyl)piperidin-4-yl)-N-hydroxyacetamidine and 4-phenylbenzoyl chloride.

Sources & evidence

ORD record
ord-040e032c6dcf4e81a7a182d5ed918dae
Source dataset
uspto-grants-2010_09
Patent number
US07799924B2

Reaction notes

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