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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2234384Generated: October 31, 2026

Diisopropylethylamine → 4-amino-N-(1-methylpiperidin-4-yl)-3-(trifluoromethoxy)benzamide

https://huagongshe.com/reaction/2234384

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant4-amino-3-(trifluoromethoxy)benzoic AcidHCID 2735951—
Reactant4-Amino-1-methylpiperidineHCID 2737531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
SolventDimethylformamideHCID 6228—
Product4-amino-N-(1-methylpiperidin-4-yl)-3-(trifluoromethoxy)benzamideHCID 5801515278%

Reaction Steps

To a solution of 4-amino-3-(trifluoromethoxy)benzoic acid (Maybridge; 1.05 g, 4.75 mmol) in DMF (20 ml) was added 4-amino-1-methylpiperidine (Fluorochem; 604 mg, 5.29 mmol) followed by DIPEA (1.6 ml, 9.19 mmol) and HATU (2.06 g, 5.42 mmol). The reaction mixture was stirred at ambient temperature O/N. The reaction mixture was evaporated to dryness and the residue partitioned between DCM (75 mL) and saturated aqueous sodium bicarbonate solution (75 mL). The aqueous phase was re-extraced with DCM (50 ml) and the combined organic phases washed with brine, dried over magnesium sulphate, filtered and evaporated to give the title compound as an amber gum (1.17 g, 78%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07709471B2
Source datasetuspto-grants-2010_05
ORD IDord-4f4e3746f79f46fe81a335dc298ff525
Source noteuspto-grants-2010_05