2-(Trifluoromethoxy)benzoyl Chloride → HCID 69354745, compound

HRID 1836393Notes

Reaction equation

HRID 1836393 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]([F:30])([F:29])[O:19][C:20]1[CH:28]=[CH:27][CH:26]=[CH:25][C:21]=1[C:22](Cl)=[O:23]>>[F:17][C:18]([F:29])([F:30])[O:19][C:20]1[CH:28]=[CH:27][CH:26]=[CH:25][C:21]=1[C:22]([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:23]

Participants

3

Reactant 2

HCID 27772412-(Trifluoromethoxy)benzoyl ChlorideHCID 101306514-[3-Aminobenzoyl]-1-methylpiperidine

Product 1

HCID 69354745HCID 69354745, compound

Procedure

Beginning with 4-[3-aminobenzoyl]-1-methylpiperidine (25 mg, 0.115 mmol) and 2-(trifluoromethoxy)benzoyl chloride (37 μL, 0.229 mmol) and mixing for 24 h, 49.8 mg (>100%) of the title compound were recovered.

Workup

  1. additionmixing for 24 h
  2. custom49.8 mg (>100%) of the title compound were recovered

Sources & evidence

ORD record
ord-c70de7d3821f41cdac72f9c3240024c5
Source dataset
uspto-grants-2004_08
Patent number
US06777428B1

Reaction notes

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