HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfuric Acid → 6-Amino-3-chloro-2-(4-methyl-piperazine-1-sulfonyl)-phenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 2-tert-Butyl-6-chloro-7-(4-methylpiperazine-1-sulfonyl)-benzooxazole | HCID 23447836 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 6-Amino-3-chloro-2-(4-methyl-piperazine-1-sulfonyl)-phenol | HCID 23447857 | 68% |
Reaction Steps
4.27 ml (0.08 mol; 1.20 V) of sulfuric acid diluted in 4.3 ml of water were added dropwise to 3.56 g of 2-tert-butyl-6-chloro-7-(4-methylpiperazine-1-sulfonyl)benzooxazole (0.01 mol; 1.0 eq) in solution in 15 ml of 1,4-dioxane. The reaction medium was refluxed for six and a half hours. The reaction medium was concentrated and 1 N sodium hydroxide was added (to pH 7). The solution was extracted with dichloromethane. The organic phases were combined, dried over magnesium sulfate, filtered and evaporated. The residue obtained was chromatographed on silica gel, eluent 95/5 ethyl acetate/dichloromethane. 2.0 g of 6-amino-3-chloro-2-(4-methylpiperazine- 1-sulfonyl)phenol were obtained in the form of a thick brown oil. Yield=68%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09388149B2 |
| Source dataset | uspto-grants-2016_07 |
| ORD ID | ord-b0f01e5a22d94a8c8a0634ded48fc5dd |
| Source note | uspto-grants-2016_07 |