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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 47237Generated: October 26, 2026

Formaldehyde → 1-Morpholin-4-ylmethyl-3-(1H-pyrrol-2-ylmethylene)-1,3-dihydro-indol-2-one

https://huagongshe.com/reaction/47237

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantMorpholineHCID 8083—
Reactant(Z)-3-((1H-pyrrol-2-yl)methylene)indolin-2-oneHCID 5908088—
SolventEthanolHCID 702—
Solvent1,4-DioxaneHCID 31275—
Product1-Morpholin-4-ylmethyl-3-(1H-pyrrol-2-ylmethylene)-1,3-dihydro-indol-2-oneHCID 6886588750%

Reaction Steps

A mixture of Z-(1H-Pyrrol-2-ylmethylene)-1,3-dihydro-indol-2-one (120 mg, 0.57 mmol), paraformaldehyde (32 mg, 1.1 mmol), and morpholine (62.2 μL, 0.71 mmol) in 8.0 mL of 20% dioxane in EtOH was heated at reflux for 19.5 h. The reaction mixture was concentrated and paraformaldehyde (10.0 mg, 0.33 mmol), morpholine (15 μL, 0.17 mmol) and EtOH (7 mL) was added. The reaction mixture refluxed for 24 h. The reaction mixture was cooled to room temperature and concentrated. The residue was dissolved in 15 mL of CHCl3 and treated with activated charcoal. The resulting suspension was filtered and the filtrate concentrated. The residue was crystallization from ethyl acetate/hexane to give the title compound (88.0 mg, 50%) as a bright yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06699863B1
Source datasetuspto-grants-2004_03
ORD IDord-7796d9be31304c5281081c9b2e12dd9e
Source noteuspto-grants-2004_03