HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminothiazole → 1,2-Difluoro-4-(2-nitrophenoxy)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminothiazole | HCID 2155 | — |
| Reactant | 1-Fluoro-2-nitrobenzene | HCID 73895 | — |
| Reactant | 3,4-Difluorophenol | HCID 75927 | — |
| Reactant | HCID 43554656 | HCID 43554656 | — |
| Product | 1,2-Difluoro-4-(2-nitrophenoxy)benzene | HCID 52438075 | 60% |
| Product | HCID 59732788 | HCID 59732788 | 60% |
Reaction Steps
2-(3,4-Difluorophenoxy)-1-nitrobenzene (0.76 g, 60%) was prepared from 3,4-difluorophenol (0.65 g, 5.5 mmol) and 1-fluoro-2-nitrobenzene (0.71 g, 5.0 mmol) following the general procedure A. This was reduced to 2-(3,4-difluorophenoxy)aniline (0.33 g, 60%, 2.5 mmol scale) following general procedure B. N-[2-(3,4-Difluorophenoxy)phenyl]-N′-(thiazol-2-yl)urea (312 mg, 60%) was prepared from 2-(3,4-difluorophenoxy)aniline (330 mg, 1.5 mmol) and 2-aminothiazole (150 mg, 1.5 mmol) following the general procedure D.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07541373B2 |
| Source dataset | uspto-grants-2009_06 |
| ORD ID | ord-2ccdc137b5a945c48795abe6c7568963 |
| Source note | uspto-grants-2009_06 |