HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → N-(2,6-diisopropylphenyl)-2-[1-(4-methanesulfonyl-phenyl)-2,4-dioxo-1,3-diazaspiro[4.5]dec-3-yl]acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Reactant | 2-[1-(4-cyanophenyl)-2,4-dioxo-1,3-diaza-spiro[4.5]dec-3-yl]-N-(2,6-diisopropylphenyl)acetamide | HCID 46892480 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-(2,6-diisopropylphenyl)-2-[1-(4-methanesulfonyl-phenyl)-2,4-dioxo-1,3-diazaspiro[4.5]dec-3-yl]acetamide | HCID 46892483 | — |
Reaction Steps
0.421 g (0.684 mmol; 2.2 eq.) of oxone is added to a solution of 0.158 g (0.311 mmol; 1 eq.) of N-(2,6-diisopropylphenyl)-2-[1-(4-methylsulfanylphenyl)-2,4-dioxo-1,3-diazaspiro[4.5]dec-3-yl]acetamide (prepared according to Example 2) in 5 ml of methanol and 2 ml of demineralized water. The reaction medium is stirred at room temperature for 18 hours. Water and dichloromethane are added, and the organic phase is washed several times with water, dried over sodium sulfate and then concentrated to dryness. The product N-(2,6-diisopropylphenyl)-2-[1-(4-methanesulfonyl-phenyl)-2,4-dioxo-1,3-diazaspiro[4.5]dec-3-yl]acetamide is obtained in the form of a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08420682B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-45627f7dc80c46d09c41cf6f169bad0a |
| Source note | uspto-grants-2013_04 |