HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-[2-(5-cyano-2-benzyloxyphenoxy)ethyl]-4-(1-t-butoxycarbonyl-4-piperidyloxy)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-{[1-(tert-Butoxycarbonyl)piperidin-4-yl]oxy}benzoic acid | HCID 2794649 | — |
| Reactant | 3-(2-Aminoethoxy)-4-benzyloxybenzonitrile hydrochloride | HCID 22645190 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-[2-(5-cyano-2-benzyloxyphenoxy)ethyl]-4-(1-t-butoxycarbonyl-4-piperidyloxy)benzamide | HCID 22645130 | — |
Reaction Steps
1.06 g (3.50 mmol) of 3-(2-aminoethoxy)-4-benzyloxybenzonitrile hydrochloride was dissolved in 15 ml of DMF. 1.23 g (3.84 mmol) of 4-(1-t-butoxycarbonyl-4-piperidyloxy)benzoic acid, 710 mg (4.2 mmol)) of 2-chloro-1,3-dimethylimidazonium chloride and 1.45 ml (5.19 mmol) of triethylamine were added to the obtained solution, and they were stirred overnight. After the treatment with dichloromethane as the extraction solvent in an ordinary manner, the solvent was evaporated, and the obtained residue was purified by the silica gel column chromatography to obtain the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06410538B2 |
| Source dataset | uspto-grants-2002_06 |
| ORD ID | ord-7a2723f2ea2443069ec40b3f1a5221a5 |
| Source note | uspto-grants-2002_06 |