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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1784146Generated: November 1, 2026

Pyridine → N-(3,4-Dimethoxy-phenyl)-N'-methyl-2-phenyl-N-[2-(4-trifluoromethyl-phenyl)-ethyl]-malonamide

https://huagongshe.com/reaction/1784146

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantMethylamineHCID 6329—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
ReactantN-(3,4-Dimethoxy-phenyl)-2-phenyl-N-[2-(4-trifluoromethyl-phenyl)-ethyl]-malonamic acidHCID 57591457—
SolventDimethylformamideHCID 6228—
ProductN-(3,4-Dimethoxy-phenyl)-N'-methyl-2-phenyl-N-[2-(4-trifluoromethyl-phenyl)-ethyl]-malonamideHCID 2501447916.3%

Reaction Steps

A mixture of 16.2 mg (0.033 mmol) N-(3,4-Dimethoxy-phenyl)-2-phenyl-N-[2-(4-trifluoromethyl-phenyl)-ethyl]-malonamic acid, 15.5 mg (0.049 mmol) methylamine (commercially available), 13.8 mg (0.043 mmol) TBTU and 7.8 mg (0.09 mmol) pyridine in 2 mL DMF was shaken for 4 h at room temperature. The mixture was evaporated to dryness, taken up in methanol, formic acid and subjected to purification by preparative HPLC on reversed phase eluting with a gradient formed from acetonitrile, water and acetic acid. The combined product fractions were evaporated to dryness to yield 2.7 mg (16%) of the title compound. MS(m/e): 501.3 (MH+), MH+ found: 501.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07501541B2
Source datasetuspto-grants-2009_03
ORD IDord-4b9d3f93ebc54ec0bf7376c8f134501f
Source noteuspto-grants-2009_03