HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-tert-Butylbenzenesulfonamide → HCID 19095805, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-tert-Butylbenzenesulfonamide | HCID 222872 | — |
| Reactant | HCID 19095786 | HCID 19095786 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 19095805 | HCID 19095805 | — |
Reaction Steps
A solution of 0.353 g of 4,6-dichloro-5-(2-methoxyphenoxy)-2-(thiophen-2-yl)-pyrimidine in 5 ml of DMSO was heated to 150° C. with 0.376 g of p-tert-butylbenzenesulphonamide for 30 minutes. The solution was concentrated in a high vacuum and the oily residue was poured on to ice, made acid (pH=3) and the suspension was extracted with ethyl acetate. The organic extracts were combined, washed with water, dried over sodium sulfate and concentrated under reduced pressure. The residue was chromatographed on silica gel with toluene-ethyl acetate 9:1 and yielded 4-tert-butyl-N-[6-chloro-5-(2-methoxyphenoxy)-2-(thiophen-2-yl)-pyrimidin-4-yl]-benzenesulphonamide as a white foam.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05292740 |
| Source dataset | uspto-grants-1994_03 |
| ORD ID | ord-90eb69fc4acb4edca6c9145ec56f7e3e |
| Source note | uspto-grants-1994_03 |