3,4,5-Trifluorobenzoyl chloride → 4-[3-(3,4,5-Trifluorobenzamidyl)benzoyl]-1-methylpiperidine

HRID 1836401Notes

Reaction equation

HRID 1836401 reaction equation
[NH2:1][C:2]1[CH:3]=[C:4]([CH:14]=[CH:15][CH:16]=1)[C:5]([CH:7]1[CH2:12][CH2:11][N:10]([CH3:13])[CH2:9][CH2:8]1)=[O:6].[F:17][C:18]1[CH:19]=[C:20]([CH:24]=[C:25]([F:28])[C:26]=1[F:27])[C:21](Cl)=[O:22]>>[F:17][C:18]1[CH:19]=[C:20]([CH:24]=[C:25]([F:28])[C:26]=1[F:27])[C:21]([NH:1][C:2]1[CH:3]=[C:4]([CH:14]=[CH:15][CH:16]=1)[C:5]([CH:7]1[CH2:8][CH2:9][N:10]([CH3:13])[CH2:11][CH2:12]1)=[O:6])=[O:22]

Participants

3

Reactant 2

HCID 27770233,4,5-Trifluorobenzoyl chlorideHCID 101306514-[3-Aminobenzoyl]-1-methylpiperidine

Product 1

HCID 235188164-[3-(3,4,5-Trifluorobenzamidyl)benzoyl]-1-methylpiperidineYield 99%

Procedure

Following the example above and beginning with 4-[3-aminobenzoyl]-1-methylpiperidine (25 mg, 0.115 mmol) and 3,4,5-trifluorobenzoyl chloride (30 μL, 0.229 mmol), 42.5 mg (99%) of the title compound were recovered.

Sources & evidence

ORD record
ord-43f3879cfabd408989adf9b201bbebc7
Source dataset
uspto-grants-2004_08
Patent number
US06777428B1

Reaction notes

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