HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 4-[(glycylamino)methyl]-1-[4-(N-phenylcarbamoyl)benzyl]piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| 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
An acetonitrile (100 mL) solution of 4-(N-phenylcarbamoyl)benzyl chloride (800 mg, 3.26 mmol) was dropped into a mixture of 4-[[N-(9-fluorenylmethyloxycarbonyl)glycyl]aminomethyl]piperidine (1.27 g, 2.96 mmol) with triethylamine (1.25 mL, 8.88 mmol), KI (50 mg, 0.30 mmol) and acetonitrile (200 mL). The resulting mixture was stirred at room temperature for 19 hours and stirred at 60° C. for another 5 hours. After concentrating, the obtained crude product was purified by column chromatography (SiO2, 5% methanol/dichloromethane-triethylamine/methanol/dichloromethane=2:2:96) to provide 4-[(glycylamino)methyl]-1-[4-(N-phenylcarbamoyl)benzyl]piperidine (340 mg, 30%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07390830B1 |
| Source dataset | uspto-grants-2008_06 |
| ORD ID | ord-0f213beb0cf7442493f52ba91697ded6 |
| Source note | uspto-grants-2008_06 |