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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1966235Generated: October 30, 2026

1-Methyl-3-aminopyrazole → HCID 25261183, compound

https://huagongshe.com/reaction/1966235

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Methyl-3-aminopyrazoleHCID 137254—
ReactantHCID 86644606HCID 86644606—
CatalystHCID 178482626HCID 178482626—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 25261183HCID 2526118355%

Reaction Conditions

Temperature80 °C

Reaction Steps

2-Bromo-5-(4-methanesulfonyl-phenoxy)-pyridine (0.47 mmol), sodium-tert.-butylate (1.4 eq.), and 1-methyl-1H-pyrazole-3-amine (1.2 eq.) are dissolved in degassed dioxane (2.5 ml) and heated to 80° C. Chloro(di-2-norbornylphosphino)(2-dimethylaminoferrocene-1-yl)palladium (II) (5.9 mg) in degassed dioxane (1 ml) is added and the reaction mixture is heated for 1 hour at 142° C. in the microwave. The reaction is quenched with ethylacetate (30 ml) and filtrated over celite. The solvent of the filtrate is removed in vacuo [5-(4-Methanesulfonyl-phenoxy)-pyridine-2-yl]-(1-methyl-1H-pyrazole-3-yl)-amine (“A27”) is obtained after reversed phase column chromatography (water/acetonitrile+0.1% TFA) as orange powder in a yield of 55%; HPLC (method C): 1.57 min; LC-MS (method A): 0.787 min, 345.15 (M+H+);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08420642B2
Source datasetuspto-grants-2013_04
ORD IDord-0745bec8d1cb4998af06f4655b906f46
Source noteuspto-grants-2013_04