HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(4-Fluorobenzoyl)piperidine → HCID 12852062, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(4-Fluorobenzoyl)piperidine | HCID 2724440 | — |
| Reactant | HCID 20278944 | HCID 20278944 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 12852062 | HCID 12852062 | 57% |
Reaction Steps
A mixture of 5.8 parts of 6-chloro-3-(2-chloroethyl)-3,4-dihydro-4-phenyl-2(1H)-quinazolinone, 7.4 parts of (4-fluorophenyl)(4-piperidinyl)methanone and 56 parts of ethanol is stirred and refluxed overnight. The reaction mixture is evaporated. The residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (95:5 by volume) as eluent. The pure fractions are collected and the eluent is evaporated. THe oily residue solidifies on triturating in 2,2'-oxybispropane. The product is filtered off and dried, yielding 5 parts (57%) of 6-chloro-3-[2-[4-(4-fluorobenzoyl)-1-piperidinyl]ethyl]-3,4-dihydro-4-phenyl-2(1H)-quinazolinone; mp. 196° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04522945 |
| Source dataset | uspto-grants-1985_06 |
| ORD ID | ord-fefdc7dddf1e44038d3dc4500bf0c18f |
| Source note | uspto-grants-1985_06 |