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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1158775Generated: October 26, 2026

4-Methylmorpholine → HCID 67014569, compound

https://huagongshe.com/reaction/1158775

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
Reactant4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chlorideHCID 2734059—
ReactantPhenylephrine HydrochlorideHCID 5284443—
ReactantHCID 10490410HCID 10490410—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67014569HCID 6701456918.3%

Reaction Steps

2-Dimethylamino-4-phenylpyrimidine-5-carboxylic acid (1.22 g, 5 mmol) is dissolved in tetrahydrofuran (60 ml). After 5 minutes of stirring to the solution are added: L-phenylephrine hydrochloride (1.22 g, 6 mmol) in tetrahydrofuran (50 ml), after another 5 minutes of stirring the N-methylmorpholine (1.21 g, 12 mmol) and after 2 minutes of stirring the 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride (1.66 g, 6 mmol). The reaction mixture is stirred for 2 hours at room temperature, then heated at reflux temperature for 2 hours. The solvent is removed in vacuum. To the residue water (50 ml) is added, and the mixture is extracted with chloroform (75 ml), the extract is washed with 10% sodium carbonate solution (35 ml), with water (35 ml), dried over sodium sulphate and evaporated. The residue is chromatographed on silicagel using chloroform-methanol 100/1-100/5 mixture eluent. 0.36 g of the title compound is obtained, m.p.: 79-81° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07812031B2
Source datasetuspto-grants-2010_10
ORD IDord-eb4f4ea8e2a549fd989d745a3e04734a
Source noteuspto-grants-2010_10