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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 917751Generated: October 26, 2026

4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride → 4-(4-bromo-2-fluoroanilino)-N-(2-hydroxyethoxy)-1-methyl-6-oxo-1,6-dihydro-3-pyridinecarboxamide

https://huagongshe.com/reaction/917751

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chlorideHCID 2734059—
ReactantEthanol, 2-(aminooxy)-HCID 3014186—
Reactant4-(4-Bromo-2-fluorophenylamino)-1-methyl-6-oxo-1,6-dihydropyridine-3-carboxylic acidHCID 11580925—
SolventMethanolHCID 887—
Product4-(4-bromo-2-fluoroanilino)-N-(2-hydroxyethoxy)-1-methyl-6-oxo-1,6-dihydro-3-pyridinecarboxamideHCID 1118877238%

Reaction Steps

2-(Aminooxy)ethanol, 4-(4-bromo-2-fluoroanilino)-1-methyl-6-oxo-1,6-dihydro-3-pyridinecarboxylic acid and DMT-MM were reacted in MeOH as outlined in example 33, step D. Further purification by flash chromatography on silica gel (EtOAc followed by 10% MeOH/CH2Cl2) gave 4-(4-bromo-2-fluoroanilino)-N-(2-hydroxyethoxy)-1-methyl-6-oxo-1,6-dihydro-3-pyridinecarboxamide (38%); m.p. (EtOAc/Hexane) 124-128° C. 1H NMR [400 MHz, (CD3)2SO] δ 11.64 (br s, 1H), 9.50 (br s, 1H), 8.13 (s, 1H), 7.69-7.65 (m, 1H), 7.47-7.41 (m, 2H), 5.53 (d, J=0.7 Hz, 1H), 4.78 (s, 1H), 3.91 (t, J=5.0 Hz, 2H), 3.61 (t, J=5.0 Hz, 2H), 3.36 (s, 3H). LCMS (ACPI−) 400 (80%), 398 (100%). Anal. Calcd for C15H15BrFN3O4.0.25 H2O: C, 44.5; H, 3.9; N, 10.4. Found C, 44.3; H, 3.5; N, 10.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07273877B2
Source datasetuspto-grants-2007_09
ORD IDord-cfa3313bdfa649e4bda7c6819ca1942b
Source noteuspto-grants-2007_09