HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(1-benzylpiperidin-4-yl)-4-(4-chlorophenyl)-3,4-dihydro-2(1H)-quinazolinone → 3-(piperidin-4-yl)-4-(4-chlorophenyl)-3,4-dihydro-2(1H)-quinazolinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(1-benzylpiperidin-4-yl)-4-(4-chlorophenyl)-3,4-dihydro-2(1H)-quinazolinone | HCID 12109389 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | 1-Chloroethyl chloroformate | HCID 521305 | — |
| Product | 3-(piperidin-4-yl)-4-(4-chlorophenyl)-3,4-dihydro-2(1H)-quinazolinone | HCID 18770891 | 97.2% |
Reaction Steps
To a solution of 1.40 g (3.25 mmol) of 3-(1-benzylpiperidin-4-yl)-4-(4-chlorophenyl)-3,4-dihydro-2(1H)-quinazolinone in methylene chloride, α-chloroethyl chloroformate was added dropwise under ice-cooling and stirred for one hour. After concentration under reduced pressure, the residue was dissolved with 28 ml of methanol and stirred at room temperature for 2 hours and under ice-cooling for one hour. The precipitated crystals were collected to give 1.08 g (3.16 mmol) of the title compound as colorless crystal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06645971B1 |
| Source dataset | uspto-grants-2003_11 |
| ORD ID | ord-e991532bd08849448ed1659524cad056 |
| Source note | uspto-grants-2003_11 |