HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-[4-(2-amino-6-chloropyrimidin-4-ylsulfamoyl)phenyl]-acetamide → 4-amino-N-(2-amino-6-chloro-pyrimidin-4-yl)-benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-[4-(2-amino-6-chloropyrimidin-4-ylsulfamoyl)phenyl]-acetamide | HCID 10736032 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 4-amino-N-(2-amino-6-chloro-pyrimidin-4-yl)-benzenesulfonamide | HCID 10732939 | 97.5% |
Reaction Steps
0.885 g (0.0026 mol) of N-[4-(2-amino-6-chloropyrimidin-4-ylsulfamoyl)phenyl]-acetamide was dissolved in 31 ml of 0.5N NaOH and boiled at reflux for 3 hours. The mixture was extracted with ethyl acetate, the aqueous phase was saturated with sodium chloride and the remaining ethyl acetate was distilled off on a rotary evaporator. Then, the aqueous phase was made acid with 3N HCl and the precipitate which separated was filtered off under suction. After drying there was obtained 0.76 g (86%) of 4-amino-N-(2-amino-6-chloro-pyrimidine-4-yl)-benzenesulfonamide as beige crystals; m.p.: >265° C. (dec.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06030976 |
| Source dataset | uspto-grants-2000_02 |
| ORD ID | ord-67c2c44d61e04950a8b8fd318843a481 |
| Source note | uspto-grants-2000_02 |