HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 2(1H)-Quinazolinone, 3,4-dihydro-3-(1-(2-(4-chlorophenyl)-2-hydroxyethyl)-4-piperidinyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 1-(4-Chlorobenzoylmethyl)-4-[3,4-dihydro-2(1H)-quinazolinon-3-yl]-piperidine | HCID 12797993 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2(1H)-Quinazolinone, 3,4-dihydro-3-(1-(2-(4-chlorophenyl)-2-hydroxyethyl)-4-piperidinyl)- | HCID 3061387 | 58.6% |
Reaction Steps
In this example, 2.70 g of 1-(4-chlorobenzoylmethyl)-4-[3,4-dihydro-2(1H)-quinazolinon-3-yl]-piperidine and 150 ml of methanol are mixed and stirred at room temperature. To the stirred mixture, 2.0 g of sodium borohydride is added over a period of 5 hours. Then, the resultant mixture is stirred overnight at room temperature. The white crystals deposited are separated by filtration, successively washed with methanol and water and dried to obtain 2.07 g of a crude product. The crude product is recrystallized from a mixed solvent of chloroform and ethanol to obtain 1.59 g of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04344948 |
| Source dataset | uspto-grants-1982_08 |
| ORD ID | ord-992b58a31d184306a098a05d791f8bd3 |
| Source note | uspto-grants-1982_08 |