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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1835653Generated: October 30, 2026

4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride → HCID 10150539, compound

https://huagongshe.com/reaction/1835653

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chlorideHCID 2734059—
ReactantEthanol, 2-(aminooxy)-HCID 3014186—
ReactantHCID 12135108HCID 12135108—
SolventMethanolHCID 887—
ProductHCID 10150539HCID 1015053979%

Reaction Steps

3,4-difluoro-2-[2-fluoro-4-(methoxycarbonyl)anilino]benzoic acid (320 mg, 0.99 mmol) was dissolved in MeOH (50 mL) to which was added 2-(aminooxy)ethanol followed by 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methymorpholinium chloride [DMT-MM, prepared according to the procedure of Kunishima et al [Tetrahedron, 55, 13159-13170 (1999)]] (326 mg, 1.18 mmol), This mixture was stirred 15 h. at room temperature. The MeOH was removed under reduced pressure and the resulting oil dissolved in EtOAc (100 mL), which was washed with water (2×100 mL), brine (100 mL) and dried (Na2SO4). The solvent was removed under reduced pressure to afford a crude yellow oil which was purified by filtration through a plug of silica gel (100% EtOAc as eluant) to give methyl 4-(2,3-difluoro-6-{[(2-hydroxyethoxy)amino]carbonyl} anilino)-3-fluorobenzoate as a cream solid (79%); m.p. (EtOAc/hexane) 162-165° C. 1H NMR [400 MHz, (CD3)2SO] δ 11.82 (v br s, 1 H), 9.08 (v br s, 1 H), 7.70-7.62 (m, 2 H), 7.49-7.43 (m, 1 H), 7.38-7.29 (m, 1 H), 6.81 (ddd, J=8.6, 8.6, 4.7 Hz, 1 H), 4.76 (v br s, 1 H), 3.83-3.78 (m, 5 H), 3.53 (t, J=4.8 Hz, 2 H). Anal. calcd. for C17H15F3N2O5: C, 53.1; H, 3.9; N, 7.3. Found C, 53.3; H, 4.2; N, 7.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06770778B2
Source datasetuspto-grants-2004_08
ORD IDord-de8279a4de854ab391896233a4165165
Source noteuspto-grants-2004_08