HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isopropanol → 3-[4-(5-t-Butyl-isoxazol-3-ylamino)-pyrimidin-2-ylamino]-benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Benzenesulfonamide, 3-amino- | HCID 7377 | — |
| Reactant | (2-Chloro-pyrimidin-4-yl)-(5-tert-butyl-isoxazol-3-yl)-amine | HCID 21936452 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 3-[4-(5-t-Butyl-isoxazol-3-ylamino)-pyrimidin-2-ylamino]-benzenesulfonamide | HCID 21936460 | — |
Reaction Conditions
| Temperature | 120 °C |
|---|
Reaction Steps
To a slurry of (5-t-butyl-isoxazol-3-yl)-(2-chloro-pyrimidin-4-yl)-amine (Example 2, Step A) (0.120 mg, 0.47 mmol) in DMSO (0.120 mL) was added 3-aminobenzenesulfonamide (0.082 g, 0.47 mmol). The reaction mixture was heated at 120° C. in a sealed tube for 1 h at which time TLC indicated the disappearance of starting material. IPA (5 mL) was added and the mixture was filtered and washed with IPA (2×1 mL) to yield the title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07115617B2 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-0553dfa72da049f8bc4ce472515ab65e |
| Source note | uspto-grants-2006_10 |