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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2040660Generated: November 2, 2026

3-({[2-amino-5-(trifluoromethyl)phenyl]carbamoyl}methyl)-N-methoxy-N-methylcyclobutane-1-carboxamide → HCID 178502665, compound

https://huagongshe.com/reaction/2040660

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-({[2-amino-5-(trifluoromethyl)phenyl]carbamoyl}methyl)-N-methoxy-N-methylcyclobutane-1-carboxamideHCID 86666118—
SolventAcetic AcidHCID 176—
ProductHCID 178502665HCID 17850266596%

Reaction Conditions

Temperature125 °C

Reaction Steps

A solution of the 3-({[2-amino-5-(trifluoromethyl)phenyl]carbamoyl}methyl)-N-methoxy-N-methylcyclobutane-1-carboxamide (0.82 g, 2.29 mmol) in AcOH (10 ml) was heated to reflux (˜125° C.) whilst stirring for 2.5 h. The reaction was monitored by LC MS. The reaction mixture was allowed to cool to RT and then evaporated in vacuo. The residue was dissolved in DCM (30 ml) and washed with sat. NaHCO3 (50 ml), dried over Na2SO4, filtered and evaporated. The crude was purified by silica gel column chromatography, eluting with MeOH:DCM (2:98-5:95) to give a yellow-brown oil (0.75 g, 94%); MS (ESI+) for C16H18F3N3O2 m/z 342.10[M+H]+; HPLC purity 97% (ret. time, 1.40 min); 1H NMR (500 MHz, MeOD) δH ppm 1.96-2.17 (2 H, m), 2.27-2.55 (2 H, m), 2.66-2.92 (1 H, m), 2.97-3.15 (2 H, m), 3.15-3.22 (3 H, m), 3.32-3.62 (1 H, m), 3.63-3.73 (3 H, m), 7.37-7.53 (1 H, m), 7.53-8.00 (2 H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580762B2
Source datasetuspto-grants-2013_11
ORD IDord-3e4f10b5142a4622acaa20e07b4f0b8f
Source noteuspto-grants-2013_11