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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2221155Generated: October 30, 2026

Pyrrolidine → HCID 66679022, compound

https://huagongshe.com/reaction/2221155

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrrolidineHCID 31268—
ReactantHCID 58916337HCID 58916337—
Solvent1,4-DioxaneHCID 31275—
SolventChloroform isopropyl alcoholHCID 21906603—
ProductHCID 66679022HCID 6667902284%

Reaction Conditions

Temperature110 °C

Reaction Steps

Combine 1-(2-chloro-ethyl)-7-[2-[6-methyl-(pyridin-2-yl)]-5,6-dihydro-4H-pyrrolo[1,2-b]pyrazol-3-yl]-1H-quinoxalin-2-one (Preparation 7; 60 mg, 0.15 mmol) and pyrrolidine (0.5 ml) in dioxane (5 mL) in a pressure tube. Seal the tube and heat at 110° C. for 40 min. Dilute the reaction mixture with 1:1 chloroform/isopropyl alcohol and wash the solution with saturated sodium chloride solution. Dry the organic phase (sodium sulfate), filter, and concentrate in vacuo. Purify the residue by silica gel chromatography (dichloromethane to 1:1 dichloromethane/methanol) to give 54 mg (84%) of the titled compound. MS ES+ m/e 441 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07368445B2
Source datasetuspto-grants-2008_05
ORD IDord-e0ecdecb54db46878328f4ae7d094b03
Source noteuspto-grants-2008_05