HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 469251Generated: October 30, 2026
Ammonium Chloride → HCID 66636981, compound
https://huagongshe.com/reaction/469251
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2-Methylpropan-2-olate | HCID 4574913 | — |
| Reactant | Potassium | HCID 5462222 | — |
| Reactant | (3-Benzyloxypropyl)triphenylphosphonium bromide | HCID 10929077 | — |
| Reactant | HCID 86633064 | HCID 86633064 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66636981 | HCID 66636981 | 99.6% |
Reaction Steps
To a 20 ml THF suspension of 1081 mg of (3-benzyloxypropyl)triphenylphosphonium bromide was added 258 mg of potassium, tert-butoxide followed by stirring for 1.5 hours. A 10 ml THF solution of 358 mg of 7-(cyclohexylamino)-1-(1-ethylpropyl)-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carbaldehyde was added thereto, followed by stirring for 1 hour. To the reaction mixture was added aqueous saturated ammonium chloride, followed by extraction with ethyl acetate and washing with aqueous saturated sodium chloride. After drying over anhydrous sodium sulfate and subsequent concentration under a reduced pressure, the residue was purified by silica gel column chromatography to obtain 488 mg of 3-[4-(benzyloxy)but-1-en-1-yl]-7-(cyclohexylamino)-1-(1-ethylpropyl)-6-fluoroquinolin-4(1H)-one.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08629126B2 |
|---|
| Source dataset | uspto-grants-2014_01 |
|---|
| ORD ID | ord-f386f690384a4225b083ba4e5a95032f |
|---|
| Source note | uspto-grants-2014_01 |
|---|