HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1110012Generated: November 1, 2026
N-Hydroxysuccinimide → HCID 15231858, compound
https://huagongshe.com/reaction/1110012
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Hydroxysuccinimide | HCID 80170 | — |
| Reactant | HCID 11130710 | HCID 11130710 | — |
| Reactant | HCID 19018666 | HCID 19018666 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 15231858 | HCID 15231858 | 67% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05324728 |
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| Source dataset | uspto-grants-1994_06 |
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| ORD ID | ord-4d867e811f824e4e948eaea6c69cd6e9 |
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| Source note | uspto-grants-1994_06 |
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