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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | trans-N,N'-dimethyl-1,2-cyclohexanediamine | HCID 2733821 | — |
| Reactant | 4-[2-(3-Iodophenoxy)ethyl]morpholine | HCID 18403555 | — |
| Reactant | HCID 178439404 | HCID 178439404 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3-Isopropyl-1-(3-(2-morpholinoethoxy)phenyl)-1H-pyrazol-5-amine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09249125B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-be5c611864ad4ccc91bacf8fab260a8f |
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| Source note | uspto-grants-2016_02 |
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