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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1832086Generated: October 30, 2026

4-Methylmorpholine → HCID 22050287, compound

https://huagongshe.com/reaction/1832086

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantAmmonium HydroxideHCID 14923—
Reactant2-Chloro-4,6-dimethoxy-1,3,5-triazineHCID 18450—
ReactantHCID 22050518HCID 22050518—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22050287HCID 2205028765%

Reaction Steps

A 250 mL round bottomed flask equipped with stirbar and nitrogen inlet was charged with 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-fluorobenzoic acid (3.65 g, 7.8 mmol), 4-methylmorpholine (2.6 mL, 23.4 mmol), 2-chloro-4,6-dimethoxy-1,3,5-triazine (1.64 g, 9.36 mmol) and tetrahydrofuran (40 mL). After stirring the mixture for 30 min at 250 C, NH4OH (20.0 mL) was added. The mixture was stirred for 30 min and diluted with water. The product precipitated from solution. The precipitated was filtered and washed with water and diethyl ether to give the title compound (2.37 g, 65%) as a white solid. 1H NMR (400 MHz, (CD3)2SO) δ 7.9 (d, J=7.3 Hz, 1H), 7.61 (q, J=8.6 and 6.7 Hz, 1H), 7.5 (m, 2H), 7.3 (t, J=9.6 Hz, 1H), 7.15 (t, J=8.7 Hz, 1H), 6.7 (s, 1H), 5.36 (s, 2H), 2 (s, 3H) ppm. ES-HRMS m/z 469.0172 (M+H calcd for C20H15BrF3N2O3 requires 469.0195).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07067540B2
Source datasetuspto-grants-2006_06
ORD IDord-228a69811335452b87a07624c0013062
Source noteuspto-grants-2006_06