HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1894858Generated: October 26, 2026
Water → N-(2,6-diisopropylphenyl)-2-(2,2-dioxo-1-phenyl-2-thia-1,3-diazaspiro[4.5]dec-3-yl]acetamide
https://huagongshe.com/reaction/1894858
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Chloro-N-(2,6-diisopropylphenyl)acetamide | HCID 2363774 | — |
| Reactant | 1-Phenyl-2-thia-1,3-diazaspiro[4.5]decane-2,2-dioxide | HCID 68630732 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-(2,6-diisopropylphenyl)-2-(2,2-dioxo-1-phenyl-2-thia-1,3-diazaspiro[4.5]dec-3-yl]acetamide | HCID 25226976 | 53% |
Reaction Steps
75 mg (0.54 mmol) of potassium carbonate are added to a solution of 130 mg (0.49 mmol) of 1-phenyl-2-thia-1,3-diazaspiro[4.5]decane-2,2-dioxide and 136 mg (0.54 mmol) of 2-chloro-N-(2,6-diisopropylphenyl)-acetamide in 30 ml of dimethylformamide. The reaction medium is stirred at room temperature for one night and then it is heated to reflux for 6 hours and at room temperature for 48 h. The medium is then poured into water and extracted with ethyl acetate. The organic phases are collected and washed with water. They are dried over sodium sulfate. The solvents are evaporated. The residue is chromatographed on silica gel (heptane/ethyl acetate 90/10). 125 mg of N-(2,6-diisopropylphenyl)-2-(2,2-dioxo-1-phenyl-2-thia-1,3-diazaspiro[4.5]dec-3-yl]acetamide are obtained in the form of a yellow oil. The product is triturated in dichloromethane and plenty of heptane. A solid is obtained. M.p. 140-2° C., yield=53%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08513307B2 |
|---|
| Source dataset | uspto-grants-2013_08 |
|---|
| ORD ID | ord-79a5fb6caafa43a28a312bc2dfa1098e |
|---|
| Source note | uspto-grants-2013_08 |
|---|