4-(Trifluoromethoxy)benzoyl Chloride → HCID 68804492, compound

HRID 1715754Notes

Reaction equation

HRID 1715754 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].[F:17][C:18]([F:30])([F:29])[O:19][C:20]1[CH:28]=[CH:27][C:23]([C:24]([Cl:26])=O)=[CH:22][CH:21]=1>>[ClH:26].[CH2:1]([CH:3]([N:6]1[CH2:11][CH2:10][CH:9]([CH2:12][C:13]2[N:14]=[C:24]([C:23]3[CH:27]=[CH:28][C:20]([O:19][C:18]([F:17])([F:29])[F:30])=[CH:21][CH:22]=3)[O:16][N:15]=2)[CH2:8][CH2:7]1)[CH2:4][CH3:5])[CH3:2]

Participants

3

Reactant 2

HCID 1421104-(Trifluoromethoxy)benzoyl ChlorideHCID 178446096HCID 178446096, compound

Product 1

HCID 68804492HCID 68804492, 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-trifluoromethoxybenzoyl chloride.

Sources & evidence

ORD record
ord-71cf6c916ad44dd58d5320ee8ed887d6
Source dataset
uspto-grants-2010_09
Patent number
US07799924B2

Reaction notes

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