HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,3-dichloro-N-(3,5-dichloro-2-pyrazinyl)benzenesulphonamide → N-[3-[(2-amino-4-oxazolyl)methoxy]-5-chloro-2-pyrazinyl]-2,3-dichlorobenzenesulphonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,3-dichloro-N-(3,5-dichloro-2-pyrazinyl)benzenesulphonamide | HCID 10126340 | — |
| Reactant | tert-Butyl (4-(hydroxymethyl)oxazol-2-yl)carbamate | HCID 45092179 | — |
| Product | N-[3-[(2-amino-4-oxazolyl)methoxy]-5-chloro-2-pyrazinyl]-2,3-dichlorobenzenesulphonamide | HCID 10310503 | — |
Reaction Steps
Prepared by the method of Example 112 using (4-hydroxymethyl-2-oxazolyl)carbamic acid tert-butyl ester (Example 212a) (0.12 g) and 2,3-dichloro-N-(3,5-dichloro-2-pyrazinyl)benzenesulphonamide (Example 74) (0.21 g). Purification was by silica gel chromatography eluting with ethyl acetate/iso-hexane mixtures to give the title compound with the BOC (tert-butyl carbonyl) attached (0.11 g). This compound was dissolved in trifluoroacetic acid (1.5 mL) and dichloromethane (1.5 mL). After 2 h, the solution was evaporated. Purification was by silica gel chromatography eluting with ethyl acetate/iso-hexane mixtures to give the title compound. Yield 0.08 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07662825B2 |
| Source dataset | uspto-grants-2010_02 |
| ORD ID | ord-4a4421fd9da24a00b6c627c64bbfad4c |
| Source note | uspto-grants-2010_02 |