HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → HCID 21948133, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | HCID 21948180 | HCID 21948180 | — |
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Reactant | Bentonite | HCID 71586775 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 21948133 | HCID 21948133 | 46% |
Reaction Steps
To a solution of montmorillonite K10 (107.5 mg) in CHCl3 was added 13 uL of water. 2-anilino-7-(butylsulfanyl)-1-phenyl-5-(trifluoromethyl)-1,8-naphthyridin-4(1H)-one (25 mg, 0.06 mmol) was then added followed by oxone (85.2 mg, 0.14 mmol). The reaction was allowed to stir for 24 h at room temperature. After 24 h the solution was bright bluish-green in color and was filtered and washed with copious amounts of CHCl3. The filtrate was then concentrated in vacuo. Silica gel flash chromatography using 3:1 Hex:EtOAc provided 2-anilino-7-(butylsulfonyl)-1-phenyl-5-(trifluoromethyl)-1,8-naphthyridin-4(1H)-one as a yellow oil (13.8 mg, 46%): LCMS RT: 3.14, MH+ 502.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07109196B2 |
| Source dataset | uspto-grants-2006_09 |
| ORD ID | ord-e6d9bed45ec549c0a00cf22d65ed0f61 |
| Source note | uspto-grants-2006_09 |