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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 907415Generated: October 25, 2026

n-Methyl-4-(trifluoromethoxy)aniline → N'-[4,6-bis(2,2,2-trifluoroethoxy)pyrimidin-2-yl]-N-methyl-N-[4-(trifluoromethoxy)phenyl]urea

https://huagongshe.com/reaction/907415

Reaction equation

Participants

RoleNameHCIDCharge
Reactantn-Methyl-4-(trifluoromethoxy)anilineHCID 737351—
Reactant2-Isocyanato-4,6-bis(2,2,2-trifluoroethoxy)pyrimidineHCID 57651797—
SolventDichloromethaneHCID 6344—
ProductN'-[4,6-bis(2,2,2-trifluoroethoxy)pyrimidin-2-yl]-N-methyl-N-[4-(trifluoromethoxy)phenyl]ureaHCID 5765168638.6%

Reaction Steps

To a solution of 2-isocyanato-4,6-bis(2,2,2-trifluoroethoxy)pyrimidine (400 mg, 1.26 mmol) in CH2Cl2 (1 mL) was added a solution of N-methyl-4-(trifluoromethoxy)aniline (285 mg, 1.50 mmol) in CH2Cl2 (2 mL). The resulting solution was stirred 18 h and then concentrated. The resulting residue was purified by column chromatography (silica, hexanes/EtOAc) to afford 7 as a white solid (247 mg, 38% yield): m.p. 100-102° C.; 1H NMR (CDCl3) δ 7.39 (app s, 4H), 5.96 (s, 1H), 6.82 (bs, 1H), 4.77-4.69 (q, 4H, J=8.5 Hz); ESI/MS 509 (M+H), 507 (M−H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08013154B2
Source datasetuspto-grants-2011_09
ORD IDord-2945671dfde44ad39dd167745d4e00fb
Source noteuspto-grants-2011_09