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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1361673Generated: October 29, 2026

2-(4-Methylpiperazin-1-yl)-5-(trifluoromethyl)aniline → N-(3-methyl-4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)phenyl)-N'-(2-(4-methyl-1-piperazinyl)-5-(trifluoromethyl)phenyl)urea

https://huagongshe.com/reaction/1361673

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-Methylpiperazin-1-yl)-5-(trifluoromethyl)anilineHCID 693288—
ReactantPhenyl 3-methyl-4-(3-(2-(methylamino)pyrimidin-4-yl)pyridin-2-yloxy)phenylcarbamateHCID 58587930—
SolventTetrahydrofuranHCID 8028—
ProductN-(3-methyl-4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)phenyl)-N'-(2-(4-methyl-1-piperazinyl)-5-(trifluoromethyl)phenyl)ureaHCID 58588304—

Reaction Conditions

Temperature80 °C

Reaction Steps

To phenyl 3-methyl-4-(3-(2-(methylamino)pyrimidin-4-yl)pyridin-2-yloxy)phenylcarbamate (59 mg, 0.14 mmol) in THF (1 mL) was added 2-(4-methylpiperazin-1-yl)-5-(trifluoromethyl)benzenamine (30 mg, 0.12 mmol). The mixture was stirred for 40 hours at 80° C. The crude material was purified by silica gel chromatography (0-20% MeOH/CH2Cl2) to yield the title compound as a light yellow solid. MS m/z=593 [M+H]+. Calc'd for C30H31F3N8O2: 592.63.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07880000B2
Source datasetuspto-grants-2011_02
ORD IDord-9a527f5638c44bb786f706bf6f144549
Source noteuspto-grants-2011_02