3-(Trifluoromethyl)benzoyl chloride → HCID 68805551, compound

HRID 2055682Notes

Reaction equation

HRID 2055682 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:29])([F:28])[C:19]1[CH:20]=[C:21]([CH:25]=[CH:26][CH:27]=1)[C:22]([Cl:24])=O>>[ClH:24].[CH2:1]([CH:3]([N:6]1[CH2:11][CH2:10][CH:9]([CH2:12][C:13]2[N:14]=[C:22]([C:21]3[CH:25]=[CH:26][CH:27]=[C:19]([C:18]([F:17])([F:28])[F:29])[CH:20]=3)[O:16][N:15]=2)[CH2:8][CH2:7]1)[CH2:4][CH3:5])[CH3:2]

Participants

3

Reactant 2

HCID 752573-(Trifluoromethyl)benzoyl chlorideHCID 178446096HCID 178446096, compound

Product 1

HCID 68805551HCID 68805551, 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 3-trifluoromethylbenzoyl chloride.

Sources & evidence

ORD record
ord-51589ef70791414aa2991abde32adf5c
Source dataset
uspto-grants-2008_02
Patent number
US07332508B2

Reaction notes

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