Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1771390Generated: October 26, 2026

Nitrogen → 3-Isopropyl-1-(3-(2-morpholinoethoxy)phenyl)-1H-pyrazol-5-amine

https://huagongshe.com/reaction/1771390

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantPotassium CarbonateHCID 11430—
Reactanttrans-N,N'-dimethyl-1,2-cyclohexanediamineHCID 2733821—
Reactant4-[2-(3-Iodophenoxy)ethyl]morpholineHCID 18403555—
ReactantHCID 178439404HCID 178439404—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventTolueneHCID 1140—
Product3-Isopropyl-1-(3-(2-morpholinoethoxy)phenyl)-1H-pyrazol-5-amineHCID 90004229—

Reaction Steps

To a solution of 4-(2-(3-iodophenoxyl)ethyl)morpholine (1.0 g, 2.9 mmol) in anhydrous toluene (20 mL) was added 3-isopropyl-1H-pyrazol-5-amine (397 mg, 3.17 mmol) followed by (1R,2R)—N1,N2-dimethylcyclohexane-1,2-diamine (227 μL, 1.44 mmol) and potassium carbonate (1.99 g, 14.4 mmol). The mixture was purged with N2, copper(I) iodide (82 mg, 0.43 mmol) was added and the reaction mixture was heated at reflux under N2 for 64 hr. The resulting mixture was cooled to RT and was partitioned between EtOAc and water (100 mL). The organic layer was separated and washed with brine (2×100 mL) and was then dried and evaporated in vacuo. The residue was purified by flash column chromatography (SiO2, 40 g, 0-20% MeOH in DCM, gradient elution) to afford the title compound, Intermediate A13, as a brown oil (325 mg, 33%); Rt 1.66 min (Method 2, basic); m/z 329 (M+H)+ (ES+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249125B2
Source datasetuspto-grants-2016_02
ORD IDord-be5c611864ad4ccc91bacf8fab260a8f
Source noteuspto-grants-2016_02