HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 2(1H)-Quinazolinone, 3,4-dihydro-3-(1-(2-hydroxy-2-phenylethyl)-4-piperidinyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 12797991 | HCID 12797991 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2(1H)-Quinazolinone, 3,4-dihydro-3-(1-(2-hydroxy-2-phenylethyl)-4-piperidinyl)- | HCID 3061386 | 63.5% |
Reaction Steps
In this example, 2.30 g of 1-benzoylmethyl-4-[3,4-dihydro-2(1H)-quinazolinon-3-yl]-piperidine and 100 ml of methanol are mixed and stirred at room temperature. To the stirred mixture, 1.5 g of sodium borohydride is added over a period of 5 hours. Then, the 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 2.06 g of a crude product. The crude product is recrystallized from a mixed solvent of chloroform and ethanol to obtain 1.47 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-3b60b47fb05a42fd8732d7861d2d1c48 |
| Source note | uspto-grants-1982_08 |