HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → N-(((1-(2-Naphthalenylmethyl)-4-piperidinyl)amino)carbonyl)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Bromomethylnaphthalene | HCID 70320 | — |
| Reactant | 4-Benzoylureidopiperidine | HCID 12608582 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-(((1-(2-Naphthalenylmethyl)-4-piperidinyl)amino)carbonyl)benzamide | HCID 72002 | — |
Reaction Steps
4-Benzoylureidopiperidine (1.28 g, 0.005 m), 2-(bromomethyl)naphthalene (1.1 g, 0.005 m) and triethylamine (0.6 g, 0.006 m) in dimethylformamide (25 cm3) were stirred at room temperature for 23 hours. Water was added and the precipitated solid filtered off and washed well with water. The solid was suspended in warm ethanol, acidified with ethanolic HCl and then heated until all the solid had dissolved. The title compound crystallised and was collected as the hydrochloride salt, hemihydrate (1.6 g), m.p. 232°-234° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04563466 |
| Source dataset | uspto-grants-1986_01 |
| ORD ID | ord-65eec61c6fdd4c09ba745fd6a339c7cf |
| Source note | uspto-grants-1986_01 |