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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1966232Generated: October 30, 2026

1-Methyl-3-aminopyrazole → HCID 25261181, compound

https://huagongshe.com/reaction/1966232

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Methyl-3-aminopyrazoleHCID 137254—
Reactant2-Bromo-5-(cyclopentyloxy)pyridineHCID 57821690—
CatalystHCID 178482626HCID 178482626—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 25261181HCID 2526118129%

Reaction Conditions

Temperature80 °C

Reaction Steps

2-Bromo-5-cyclopentyloxy-pyridine (0.97 mmol), sodium-tert.-butylate (1.4 eq.), and 1-methyl-1H-pyrazole-3-amine (1.2 eq.) are dissolved in degassed dioxane (2 ml) and heated to 80° C. Chloro-(di-2-norbornylphosphino)(2-dimethylaminoferrocene-1-yl)palladium (II) (3 mg) in degassed dioxane (1 ml) is added and the reaction mixture is heated for 1 hour at 150° C. in the microwave. The reaction is quenched with ethylacetate/methanol (30 ml, 9:1) and filtrated over celite. The solvent of the filtrate is removed in vacuo. (5-Cyclopentyloxy-pyridine-2-yl)-(1-methyl-1H-pyrazole-3-yl)-amine (“A25”) is obtained after reversed phase column chromatography (water/acetonitrile+0.1% TEA) as a colorless powder in a yield of 29%; HPLC (method C): 1.55 min; LC-MS (method A): 0.97 min, 259.15 (M+H+);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08420642B2
Source datasetuspto-grants-2013_04
ORD IDord-d4f8b1c7e6424e87ae4d5eabe87c8c93
Source noteuspto-grants-2013_04