HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → 4-[1-(4-Cyano-3-fluorobenzyl)-5-imidazolylmethyl]-1-[3-hydroxybenzyl]-2-piperazinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 1-(4-Cyano-3-fluorobenzyl)-5-imidazolecarboxaldehyde | HCID 11424708 | — |
| Reactant | 1-[3-(Hydroxy)benzyl]-2-piperazinone hydrochloride | HCID 18536072 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 4-[1-(4-Cyano-3-fluorobenzyl)-5-imidazolylmethyl]-1-[3-hydroxybenzyl]-2-piperazinone | HCID 18536096 | — |
Reaction Steps
To a solution of the amine hydrochloride from Step K (theoretically 0.22 mmol) in 2 mL of 1,2-dichloroethane was added 4 Å powdered molecular sieves (100 mg), followed by sodium triacetoxyborohydride (70 mg, 0.33 mmol). The aldehyde from Step G (51 mg, 0.22 mmol) was added, and the reaction was stirred for 16 hours. The reaction was poured into EtOAc, washed with sat. aq. NaHCO3 and brine, dried (Na2SO4), filtered, and concentrated in vacuo. The titled product was obtained as a pale yellow foam.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06562823B1 |
| Source dataset | uspto-grants-2003_05 |
| ORD ID | ord-404df1de74b948a895ff4ee99db0dcec |
| Source note | uspto-grants-2003_05 |