HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Aminopiperidine → HCID 44390753, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Aminopiperidine | HCID 16658 | — |
| Reactant | HCID 86600271 | HCID 86600271 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 44390753 | HCID 44390753 | — |
Reaction Steps
To a portion of the methylene chloride (1 mL) solution of 2-(chloro)-6-(2,4-dichlorophenyl)-5-(4-chlorophenyl)pyridine-3-carbonyl chloride (0.068 mmol) from Step B was added a solution of 1-aminopiperidine (0.010 mL, 0.088 mmol) and TEA (0.014 mL, 0.10 mmol) in methylene chloride (1 mL). The reaction was stirred at rt for 16 h and was then evaporated. The residue was purified by preparative TLC (40% ethyl acetate in hexanes) to yield N-(piperidin-1-yl)-2-(chloro)-6-(2,4-dichlorophenyl)-5-(4-chlorophenyl)pyridine-3-carboxamide. HPLC/MS: 494 (M+1), 496 (M+3); Rt=3.97 min
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07271266B2 |
| Source dataset | uspto-grants-2007_09 |
| ORD ID | ord-8ef73c9ef99c479d981b2a50e240fba5 |
| Source note | uspto-grants-2007_09 |