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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1912397Generated: October 30, 2026

1,4-Dioxane → Jak3-IN-7

https://huagongshe.com/reaction/1912397

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DioxaneHCID 31275—
Reactant3-(3,5-Dimethyl-1H-pyrazol-1-yl)-3-oxopropanenitrileHCID 262101—
ReactantSodium BicarbonateHCID 516892—
Reactant4-(3-methyl-1,6-diazaspiro[3.5]non-6-yl)-7H-pyrrolo[2,3-d]pyrimidineHCID 58293311—
SolventWaterHCID 962—
ProductJak3-IN-7HCID 5091362021.3%

Reaction Conditions

Temperature100 °C

Reaction Steps

An optically-active compound of 4-(3-methyl-1,6-diazaspiro[3.5]non-6-yl)-7H-pyrrolo[2,3-d]pyrimidine (25 mg) was mixed with 1-cyanoacetyl-3,5-dimethylpyrazole (32 mg) and 1,4-dioxane (750 μl), and the mixture was stirred at 100° C. for 3.5 hours. The mixture was cooled to room temperature. Thereto were added water and saturated aqueous sodium bicarbonate solution, and the mixture was extracted with ethyl acetate. The separated aqueous layer was extracted with ethyl acetate five times, and the combined organic layer was washed with water and concentrated under reduced pressure. The resulting residue was purified by silica-gel thin layer chromatography (eluent: chloroform/methanol=9/1). The resulting residue was purified by silica-gel thin layer chromatography (eluent: ethyl acetate/methanol=93/7) again. The resulting solid (8.0 mg) was slurry-washed with n-hexane/ethyl acetate solution to give the titled compound (6.7 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609647B2
Source datasetuspto-grants-2013_12
ORD IDord-bf60f4d017d84c879a65993acc105b20
Source noteuspto-grants-2013_12