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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1790499Generated: November 2, 2026

1-[1-(4-Fluorophenethyl)piperidin-4-yl]-6-(ethylcarbamoylmethyl)indoline → 1-[1-(4-Fluorophenethyl)piperidin-4-yl]-6-(ethylcarbamoylmethyl)indole

https://huagongshe.com/reaction/1790499

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-[1-(4-Fluorophenethyl)piperidin-4-yl]-6-(ethylcarbamoylmethyl)indolineHCID 22038343—
CatalystHCID 178418406HCID 178418406—
SolventChloroformHCID 6212—
Product1-[1-(4-Fluorophenethyl)piperidin-4-yl]-6-(ethylcarbamoylmethyl)indoleHCID 2203837989.5%

Reaction Conditions

Temperature50 °C

Reaction Steps

A suspension of 1-[1-(4-fluorophenethyl)piperidin-4-yl]-6-(ethylcarbamoylmethyl)indoline (0.41 g) obtained in Example 149 and active manganese dioxide (0.40 g) in chloroform (30 ml) was vigorously stirred at 50° C. for 6 hr. Then the reaction mixtures were filtered through celite and the residue was washed with chloroform. After concentrating the filtrate under reduced pressure, the residue was recrystallized from chloroform/hexane to give the title compound (0.33 g) as white needles (yield: 89.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07071201B2
Source datasetuspto-grants-2006_07
ORD IDord-3bef6cddcc8f432a9aade264ee0bee09
Source noteuspto-grants-2006_07