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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1243906Generated: October 30, 2026

4-Morpholinopiperidine → (3Z)-3-({3,5-dimethyl-4-[(4-morpholin-4-ylpiperidin-1-yl)carbonyl]-1H-pyrrol-2-yl}methylene)-5-fluoro-1,3-dihydro-2H-indol-2-one

https://huagongshe.com/reaction/1243906

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MorpholinopiperidineHCID 795724—
Reactant5-fluoro-1,3-dihydro-2H-indol-2-oneHCID 3731012—
Reactant4-(1H-imidazol-1-ylcarbonyl)-3,5-dimethyl-1H-pyrrole-2-carbaldehydeHCID 21931893—
SolventTetrahydrofuranHCID 8028—
Product(3Z)-3-({3,5-dimethyl-4-[(4-morpholin-4-ylpiperidin-1-yl)carbonyl]-1H-pyrrol-2-yl}methylene)-5-fluoro-1,3-dihydro-2H-indol-2-oneHCID 1027581968.5%

Reaction Conditions

Temperature66 °C

Reaction Steps

4-(1H-imidazol-1-ylcarbonyl)-3,5-dimethyl-1H-pyrrole-2-carbaldehyde (11.3 g, 51.9 mmol), 4-morpholinopiperidine (15.0 g, 88.2 mmol), 5-fluorooxindole (7.84 g, 51.9 mmol), and THF (126 ml) were mixed and heated to 66° C. After stirring for 68 h at 66° C., the mixture was cooled to room temperature and filtered. The cake was washed with 4×20 ml THF and dried overnight at 70° C. under house vacuum. (3Z)-3-({3,5-dimethyl-4-[(4-morpholin-4-ylpiperidin-1-yl)carbonyl]-1H-pyrrol-2-yl}methylene)-5-fluoro-1,3-dihydro-2H-indol-2-one 16.09 g was obtained in 68% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07119209B2
Source datasetuspto-grants-2006_10
ORD IDord-d423ba26eb3e458a84585b20e5f4ef07
Source noteuspto-grants-2006_10