HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Nitrobenzyl bromide → HCID 19045334, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Nitrobenzyl bromide | HCID 66011 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 19045273 | HCID 19045273 | — |
| Reactant | Chloroform methanol | HCID 21584188 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 19045334 | HCID 19045334 | 59.6% |
Reaction Steps
A solution of 4-nitrobenzyl bromide (0.73 g, 3.4 mmol), 3,4-dihydro-6-acetamidospiro[(2H)-benzopyran-2,4'-piperidine]-4-one (0.94 g, 3.4 mmol) and diisopropylethylamine (0.61 ml, 3.5 mmol) in dimethylformamide (15 ml) was stirred at room temperature for 3 hr. The reaction mixture was then concentrated under reduced pressure. The residue was diluted with methylene chloride and washed with saturated sodium bicarbonate solution, water and brine. Drying and solvent evaporation gave an oil; flash chromatography (silica gel, methanol-chloroform 2/98) gave 3,4-dihydro-6-acetamido-1'-(4-nitrobenzyl)spiro[(2H)-1-benzopyran-2,4'-piperidine]-4-one (0.83 g, 59%); 75 mg converted to hydrochloride; mp>250° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05633247 |
| Source dataset | uspto-grants-1997_05 |
| ORD ID | ord-947d6841260549d3b54d67fb4a7179a9 |
| Source note | uspto-grants-1997_05 |