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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 561429Generated: October 26, 2026

2,2-Dimethyl-1,3-dioxane-4,6-dione → 5-[(4-Chloro-2-methylphenyl){5-fluoro-7-[(methylsulfanyl)methyl]-1H-indol-3-yl}methyl]-2,2-dimethyl-1,3-dioxane-4,6-dione

https://huagongshe.com/reaction/561429

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2-Dimethyl-1,3-dioxane-4,6-dioneHCID 16249—
Reactant4-Chloro-2-methylbenzaldehydeHCID 2757658—
Reactant5-Fluoro-7-[(methylsulfanyl)methyl]-1H-indoleHCID 58392227—
Catalystproline dl-formHCID 614—
SolventAcetonitrileHCID 6342—
Product5-[(4-Chloro-2-methylphenyl){5-fluoro-7-[(methylsulfanyl)methyl]-1H-indol-3-yl}methyl]-2,2-dimethyl-1,3-dioxane-4,6-dioneHCID 58392301114.3%

Reaction Steps

0.68 g (4.41 mmol) of 4-chloro-2-methylbenzaldehyde, 0.64 g (4.41 mmol) of Meldrum's acid and 24.0 mg (0.21 mmol) of D,L-proline were added to a solution of 1.00 g of the compound from Example 11A with a purity of 82% (4.20 mmol) in 35 ml of acetonitrile. The reaction mixture was stirred at RT overnight. It was concentrated, and the residue was taken up in ethyl acetate, washed with 1N hydrochloric acid, saturated aqueous sodium bicarbonate solution and water, dried over magnesium sulfate, filtered and concentrated. 2.40 g of the title compound were obtained and were reacted without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063234B2
Source datasetuspto-grants-2011_11
ORD IDord-841f5d7f1a3347af9212298297445186
Source noteuspto-grants-2011_11