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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1971033Generated: November 3, 2026

Pyridine → HCID 58096630, compound

https://huagongshe.com/reaction/1971033

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPotassium CarbonateHCID 11430—
ReactantAripiprazoleHCID 60795—
ReactantDecanoyl chlorideHCID 66982—
ReactantEthyl oxoacetateHCID 70211—
CatalystTetrabutylammonium BromideHCID 74236—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 58096630HCID 5809663038%

Reaction Steps

A mixture of Aripiprazole (2.0 g, 4.5 mmol), ethyl glyoxylate (50% soln. in toluene, 2.7 mL), K2CO3 (0.49 g, 3.6 mmol), tetrabutylammonium bromide (0.57 g, 1.8 mmol) and dichloromethane (20 mL) was heated at reflux for 4 h. The reaction mixture was cooled and quickly washed with water, dried over MgSO4 and filtered. The resulting solution was treated with pyridine (1.8 mL, 22.2 mmol) and then decanoylchloride (4.6 mL, 22.2 mmol). After being stirred for 3 h, methanol (1 mL) was added and stirred a further 10 min. The reaction mixture was washed with sat. NaHCO3 (aq), dried over MgSO4 and evaporated. The residue was purified on silica eluting with 1:1:0.1 dichloromethane/ethyl acetate/methanol to give the title compound as a yellow oil (1.2 g, 38%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431576B2
Source datasetuspto-grants-2013_04
ORD IDord-3618d60f270b4965b67036fd9f485cfa
Source noteuspto-grants-2013_04