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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2204550Generated: October 30, 2026

Sodium Hydroxide → 8-Cyclohexyl-3h-dipyrrolo[1,2-a:2',3'-e]pyrazine

https://huagongshe.com/reaction/2204550

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant8-cyclohexyl-3-tosyl-3H-dipyrrolo[1,2-a:2',3'-e]pyrazineHCID 58009993—
SolventEthyl AcetateHCID 8857—
SolventAmmonium ChlorideHCID 25517—
Solvent1,4-DioxaneHCID 31275—
Product8-Cyclohexyl-3h-dipyrrolo[1,2-a:2',3'-e]pyrazineHCID 4985021155%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of 8-cyclohexyl-3-tosyl-3H-dipyrrolo[1,2-a:2′,3′-e]pyrazine (0.015 g, 0.038 mmol) in 1,4-dioxane (3 mL) was added aqueous NaOH (2 N, 0.29 mL, 0.57 mmol). The reaction mixture was heated to about 90° C. After about 15 h, the reaction mixture was cooled to ambient temperature and diluted with EtOAc (5 mL) and saturated aqueous NH4Cl (5 mL). The organic layer was separated, washed with water (5 mL) followed by brine (5 mL), dried over anhydrous Na2SO4, filtered, and concentrated under reduced pressure. The residue was triturated with EtOAc/heptane (1:1, 1 mL). The resulting solid was collected by filtration and dried in vacuo to provide 8-cyclohexyl-3H-dipyrrolo[1,2-a:2′,3′-e]pyrazine as a tan solid (0.005 g, 55%). LC/MS (Table 2, Method a) Rt=2.78 min; MS m/z: 240 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365579B2
Source datasetuspto-grants-2016_06
ORD IDord-6a281957b33d45b488dd176c0e701b7b
Source noteuspto-grants-2016_06