HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2187821Generated: October 31, 2026
Triethylamine → 4-[(glycylamino)methyl]-1-[4-(N-phenylcarbamoyl)benzyl]piperidine
https://huagongshe.com/reaction/2187821
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-(chloromethyl)-N-phenylbenzamide | HCID 11413905 | — |
| Reactant | 4-[[N-(9-fluorenylmethyloxycarbonyl)glycyl]aminomethyl]piperidine | HCID 54359471 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-[(glycylamino)methyl]-1-[4-(N-phenylcarbamoyl)benzyl]piperidine | HCID 18426228 | 30.2% |
Reaction Steps
To a mixture of 4-[{N-(9-fluorenylmethyloxycarbonyl)glycyl}aminomethyl]piperidine (1.27 g, 2.96 mmol), Et3N (1.25 mL, 8.88 mmol), KI (50 mg, 0.30 mmol) and CH3CN (200 mL) was added dropwise a solution of 4-(N-phenylcarbamoyl)benzyl chloride (800 mg, 3.26 mmol) in CH3 CN (100 mL). The mixture was stirred at room temperature for 19 h and at 60° C. for 5 h. Concentration and column chromatography (SiO2, 5% CH3OH/CH2Cl2-Et3N:CH3OH:CH2Cl2=2:2:96) afforded 4-{(glycylamino)methyl}-1-{4-(N-phenylcarbamoyl)benzyl}piperidine (340 mg, 30%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06410566B1 |
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| Source dataset | uspto-grants-2002_06 |
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| ORD ID | ord-3c3c430eecd84d0ea67505ab53f74451 |
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| Source note | uspto-grants-2002_06 |
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