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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 561403Generated: October 31, 2026

proline dl-form → HCID 58392275, compound

https://huagongshe.com/reaction/561403

Reaction equation

Participants

RoleNameHCIDCharge
Reactantproline dl-formHCID 614—
Reactant2,2-Dimethyl-1,3-dioxane-4,6-dioneHCID 16249—
Reactant4-Chloro-2-methylbenzaldehydeHCID 2757658—
Reactant7-[(Methylsulfanyl)methyl]-1H-indoleHCID 58392187—
CatalystCopperHCID 23978—
SolventEthanolHCID 702—
SolventPyridineHCID 1049—
SolventAcetonitrileHCID 6342—
ProductHCID 58392275HCID 58392275—

Reaction Steps

1.44 g (9.31 mmol) of 4-chloro-2-methylbenzaldehyde, 1.34 g (9.31 mmol) of Meldrum's acid and 48.7 mg (0.42 mmol) of D,L-proline were added to a solution of 1.50 g (8.46 mmol) of the compound from Example 8A in 70 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 saturated aqueous sodium bicarbonate solution, water and saturated aqueous sodium chloride solution, dried over magnesium sulfate, filtered and concentrated. 3.43 g of a crude product were obtained and were introduced into 53 ml of pyridine and 14 ml of ethanol, and 4.8 mg (75 μmol) of copper powder were added. The reaction mixture was heated under reflux for 1 h. It was concentrated, and the residue was taken up in ethyl acetate, washed with 1N hydrochloric acid, dried over magnesium sulfate, filtered through silica gel and concentrated. The crude product was purified by preparative HPLC (RP18 column; mobile phase: acetonitrile/water gradient with addition of 0.1% formic acid) to result in 1.68 g (49% of theory) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063234B2
Source datasetuspto-grants-2011_11
ORD IDord-b998de4b46d24570b1c7ab418e38e89f
Source noteuspto-grants-2011_11