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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 931232Generated: November 1, 2026

Potassium Carbonate → (R)-(1-(2-(2-Cyclopropylpyrimidin-4-yl)-1H-imidazo[4,5-b]pyrazin-6-yl)piperidin-3-yl)(pyrrolidin-1-yl)methanone

https://huagongshe.com/reaction/931232

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantCesium fluorideHCID 25953—
Reactant(R)-piperidin-3-yl(pyrrolidin-1-yl)methanoneHCID 7169819—
Reactant6-Bromo-2-(2-cyclopropyl-4-pyrimidinyl)-1h-imidazo[4,5-b]pyrazineHCID 89853378—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
SolventDiglymeHCID 8150—
Product(R)-(1-(2-(2-Cyclopropylpyrimidin-4-yl)-1H-imidazo[4,5-b]pyrazin-6-yl)piperidin-3-yl)(pyrrolidin-1-yl)methanoneHCID 89857054—

Reaction Conditions

Temperature150 °C

Reaction Steps

A mixture of 6-bromo-2-(2-cyclopropylpyrimidin-4-yl)-1H-imidazo[4,5-b]pyrazine (86 mg, 0.3 mmol), (R)-piperidin-3-yl(pyrrolidin-1-yl)methanone (95 mg, 0.4 mmol), potassium carbonate (98.4, 0.7 mmol), cesium fluoride (124 mg, 0.8 mmol) and diglyme (1.0 mL) was heated to 150° C. for 3 days. The mixture was diluted with water and aqueous hydrochloric acid (1N). The mixture was extracted with ethyl acetate (3×). The combined organics were washed with brine, dried over sodium sulfate, and concentrated under reduced pressure. The residue was purified via HPLC to afford the title compound. MS (ESI+) (M+H) 419.3, HPLC retention time 2.44 min (Method A).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296745B2
Source datasetuspto-grants-2016_03
ORD IDord-bf44809cecea40d3ae4e5db7d3bdd3e7
Source noteuspto-grants-2016_03