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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1260987Generated: November 1, 2026

Diethyl Pyrocarbonate → 4-bromo-N-[(3R,4R)-3-(3,4-dichlorophenyl)-1-{[1-(hydroxyacetyl)piperidin-4-yl]carbonyl}piperidin-4-yl]-N-methylbenzamide monohydrate

https://huagongshe.com/reaction/1260987

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl PyrocarbonateHCID 3051—
ReactantTriethylamineHCID 8471—
Reactant1-Glycoloylpiperidine-4-carboxylic acidHCID 24284839—
Reactant4-bromo-N-[(3R,4R)-3-(3,4-dichlorophenyl)piperidin-4-yl]-N-methylbenzamideHCID 68930105—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product4-bromo-N-[(3R,4R)-3-(3,4-dichlorophenyl)-1-{[1-(hydroxyacetyl)piperidin-4-yl]carbonyl}piperidin-4-yl]-N-methylbenzamide monohydrateHCID 6892871994.8%

Reaction Steps

To a solution of the compound obtained in step 3 (200 mg), triethylamine (313 μL) and 1-(hydroxyacetyl)piperidine-4-carboxylic acid (101 mg) in DMF (4.5 mL) was added DEPC (87 mg), and the mixture was stirred overnight at room temperature. To the reaction mixture was added water, and the resultant product was extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium hydrogen carbonate solution, 1N hydrochloric acid and brine and dried, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (NH Chromatorex) (solvent gradient; 40→95% ethyl acetate/hexane) to give the title compound (135 mg, 49%) as a white crystal powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08470816B2
Source datasetuspto-grants-2013_06
ORD IDord-be47747f3774474bb650f508e8ee7043
Source noteuspto-grants-2013_06