Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2199518Generated: October 29, 2026

Water → HCID 86343533, compound

https://huagongshe.com/reaction/2199518

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-Chloro-5-methylpyridin-4-amineHCID 12643706—
Reactant2,2-dimethyl-6-(2-oxopropyl)-1,3-dioxin-4-oneHCID 14638420—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 86343533HCID 86343533—

Reaction Steps

To a screw top vial with rubber septa inset was added 2,2-dimethyl-6-(2-oxo-propyl)-[1,3]dioxin-4-one, prepared as described in Organic Letters, 11(21), 4910-4913; 2009, (500 mg, 2.7 mmol) and 2-chloro-5-methyl-pyridin-4-ylamine (575 mg, 4 mmol, 1.5 eq). The mixture was dissolved in anhydrous 1,4-dioxane (10 mL). Once the mixture was homogeneous the vial was placed on a stirrer/hot plate preset to 90° C. The reaction was heated at this temperature for 3.5 h. The reaction was removed from heat and analyzed by HPLC which showed the reaction was >95% complete. The vial was placed back on the hot plate. To the heated mixture was added H2SO4 (250 μL) and the reaction was heated for 1 h. The reaction was removed from the heat and after cooling to ambient temperature, the dioxane was removed by passing a stream of air over the top of the open vial to give a brown residue. Water (˜4 mL) was added to the vial, which was stirred for 30 min. The resulting tan solid was filtered off with washing from additional water and the diethyl ether to give the desired product (531 mg, 57% based on being the sulfate salt) as a tan solid which by HPLC was ˜95% pure: MS (M+H) 250.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09359300B2
Source datasetuspto-grants-2016_06
ORD IDord-e9ed6e4543df4529b6706b2730d53d9c
Source noteuspto-grants-2016_06