HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 3-Amino-5-[4-({[(2-fluoro-5-methylphenyl)amino]carbonyl}amino)phenyl]isothiazole-4-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 1-(4-(3-Amino-4-cyanoisothiazol-5-yl)phenyl)-3-(2-fluoro-5-methylphenyl)urea | HCID 86689226 | — |
| Catalyst | Hydrogen Peroxide | HCID 784 | — |
| Catalyst | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-Amino-5-[4-({[(2-fluoro-5-methylphenyl)amino]carbonyl}amino)phenyl]isothiazole-4-carboxamide | HCID 71623028 | 93% |
Reaction Steps
To a mixture of 1-[4-(3-amino-4-cyanoisothiazol-5-yl)phenyl]-3-(2-fluoro-5-methylphenyl)urea (10.2 mg, 0.028 mmol) in 0.8 mL EtOH at rt was added 15 drops 1.0M aqueous NaOH, 7 drops 30% hydrogen peroxide and the reaction stirred at rt for 30 min, then heated at 60° C. After 2.5 hours an aqueous HCl (dilute) and EtOAc workup was done to give a light yellow solid. To this material was added an impure lot from another reaction, and the combined lots triturated with EtOAc to give the title compound as a pale yellow solid (26 mg, 93% combined yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08969583B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-ec2754825a154ff5a2f8bb4b6ef7725b |
| Source note | uspto-grants-2015_03 |