Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1110012Generated: November 1, 2026

N-Hydroxysuccinimide → HCID 15231858, compound

https://huagongshe.com/reaction/1110012

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-HydroxysuccinimideHCID 80170—
ReactantHCID 11130710HCID 11130710—
ReactantHCID 19018666HCID 19018666—
SolventDichloromethaneHCID 6344—
ProductHCID 15231858HCID 1523185867%

Reaction Steps

591 mg (2.0 mM) of 5-(2-pyridylmethoxy)3-hydroxy-2-naphthoic acid was dissolved in 20 ml of dichloromethane. Thereto were added 235 mg (2.0 mM) of N-hydroxysuccinimide and 422 mg (2.0 mM) of dicyclocarbodiimide. The resulting mixture was stirred at room temperature for 1 hour. Thereto was dropwise added a solution of 620 mg (2.0 mM) of 1-(2-aminoethyl)-4-(benzhydryloxy)-piperidine in 20 ml of dichloromethane. Stirring was conducted at room temperature for 2 hours to give rise to a reaction. After the completion of the reaction, extraction with dichloromethane was conducted. The extract was washed with a saturated aqueous sodium hydrogencarbonate solution and a saturated aqueous sodium chloride solution two times, and dried over anhydrous sodium sulfate. The solvent was removed by distillation. The residue was mixed with 20 ml of acetonitrile. The mixture was filtered, and the filtrate was subjected to distillation to remove the solvent. The residue was purified by silica gel chromatography to obtain 632 mg of the title compound at a yield of 67%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05324728
Source datasetuspto-grants-1994_06
ORD IDord-4d867e811f824e4e948eaea6c69cd6e9
Source noteuspto-grants-1994_06