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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1914745Generated: October 25, 2026

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

https://huagongshe.com/reaction/1914745

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-amino-3-(trifluoromethoxy)benzoic AcidHCID 2735951—
Reactant4-Amino-1-methylpiperidineHCID 2737531—
Product4-amino-N-(1-methylpiperidin-4-yl)-3-(trifluoromethoxy)benzamideHCID 5801515271%

Reaction Steps

To a suspension of 4-amino-3-(trifluoromethoxy)benzoic acid (900 mg, 4 mmol) in dichloromethane (60 ml) TBTU (1.9 g, 6 mmol) and DIPEA (1.04 ml, 6 mmol) were added. The mixture was stirred at room temperature for 30 minutes. Then 1-methylpiperidin-4-amine (513 mg, 4.5 mmol) was added and the reaction was stirred for an additional 3 h. The solution was washed with water and the organic phase was dried over anhydrous Na2SO4. The crude was purified by flash chromatography (DCM/MeOH/NH3aq, 9:1:0.5), to give the title compound (900 mg, 71%), as an orange solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08614220B2
Source datasetuspto-grants-2013_12
ORD IDord-3e5600baa2c8498ea0eb3752c04771d8
Source noteuspto-grants-2013_12