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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1790509Generated: November 2, 2026

1-[1-(4-Fluorophenethyl)piperidin-4-yl]-6-(2-pyrrolidon-1-yl) methylindoline → 1-[1-(4-Fluorophenethyl)piperidin-4-yl]-6-(2-pyrrolidon-1-yl)methylindole

https://huagongshe.com/reaction/1790509

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-[1-(4-Fluorophenethyl)piperidin-4-yl]-6-(2-pyrrolidon-1-yl) methylindolineHCID 22038286—
CatalystHCID 178418406HCID 178418406—
SolventChloroformHCID 6212—
Product1-[1-(4-Fluorophenethyl)piperidin-4-yl]-6-(2-pyrrolidon-1-yl)methylindoleHCID 2203793186.7%

Reaction Steps

1-[1-(4-Fluorophenethyl)piperidin-4-yl]-6-(2-pyrrolidon-1-yl) methylindoline (80 mg) obtained in Example 202, activated manganese dioxide (400 mg) and chloroform (10 ml) were treated as in Example 285 to give the title compound (69 mg) as an oil. This oil was then crystallized from ethyl acetate by using oxalic acid (13 mg) to give the oxalate (54 mg) of the title compound as a white powder (yield: 61%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07071201B2
Source datasetuspto-grants-2006_07
ORD IDord-6772ea0dbccd44d99c7354c0a50d109a
Source noteuspto-grants-2006_07