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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1260981Generated: November 2, 2026

1-Hydroxybenzotriazole → HCID 68935326, compound

https://huagongshe.com/reaction/1260981

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1-(tert-Butoxycarbonyl)-4-piperidinecarboxylic acidHCID 392871—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 68935331HCID 68935331—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
SolventTriethylamineHCID 8471—
ProductHCID 68935326HCID 6893532679%

Reaction Steps

To a solution of N-[(3R,4R)-3-(3,4-dichlorophenyl)piperidin-4-yl]-N-methyl-4-morpholin-4-ylbenzamide monohydrochloride (800 mg) obtained in Example 614, step 3, 1-(tert-butoxycarbonyl)piperidine-4-carboxylic acid (566 mg) and triethylamine (684 μL) in acetonitrile (5 mL) were added WSC.HCl (473 mg) and HOBt (378 mg), and the mixture was stirred at room temperature for 14 hr. To the reaction solution was added water, and the resultant product was extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium hydrogen carbonate solution and brine and dried, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography to give the title compound (855 mg, 79%) as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08470816B2
Source datasetuspto-grants-2013_06
ORD IDord-842a5ad8cf5d44c7af44c7c4c3888784
Source noteuspto-grants-2013_06