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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 709309Generated: October 27, 2026

Potassium Carbonate → Tert-butyl 4-(4-(5-vinylpyrazin-2-ylamino)phenylsulfonyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/709309

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl 4-(4-aminophenylsulfonyl)piperazine-1-carboxylateHCID 10617209—
Reactant2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
Reactant5-Vinylpyrazin-2-amineHCID 21897256—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
ProductTert-butyl 4-(4-(5-vinylpyrazin-2-ylamino)phenylsulfonyl)piperazine-1-carboxylateHCID 6732458465.2%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 5-vinylpyrazin-2-amine (150 mg, 1.24 mmol) in 2-buOH (4 mL) were added K2CO3 (512 mg, 3.71 mmol), and tert-butyl 4-(4-aminophenylsulfonyl)piperazine-1-carboxylate (421 mg, 1.24 mmol). The reaction mixture was degassed for 10 minutes. To a mixture were added Pd2(dba)3 (76 mg, 0.07 mmol) and X-phos (53 mg, 0.11 mmol). The reaction mixture was heated to 100° C. for 6 hours after which, it was filtered with a pad of celite and partitioned between ethyl acetate and water. The organic layer was separated and the aqueous layer was extracted with ethyl acetate. The combined organic extracts were washed with brine, dried over MgSO4, celite filtered and concentrated under reduced pressure. The crude product was purified by flash chromatography using (20% to 30% Ethyl acetate/Hexane) as a solvent to afford title compound (360 mg, 65% yield). MS m/z: 446 [M+1].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09180127B2
Source datasetuspto-grants-2015_11
ORD IDord-a654ef2a4c514298b98a2219d4cb3940
Source noteuspto-grants-2015_11