HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminothiazole → 1-(4-Methoxyphenoxy)-2-nitrobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminothiazole | HCID 2155 | — |
| Reactant | 4-Methoxyphenol | HCID 9015 | — |
| Reactant | 1-Fluoro-2-nitrobenzene | HCID 73895 | — |
| Reactant | 2-(4-methoxyphenoxy)aniline | HCID 361286 | — |
| Product | 1-(4-Methoxyphenoxy)-2-nitrobenzene | HCID 668150 | 80% |
| Product | HCID 59733128 | HCID 59733128 | 75% |
Reaction Steps
2-(4-Methoxyphenoxy)-1-nitrobenzene (0.98 g, 80%) was prepared from 4-methoxyphenol (0.62 g, 5.0 mmol) and 1-fluoro-2-nitrobenzene (0.71 g, 5.0 mmol) following the general procedure A. This was reduced to 2-(4-methoxyphenoxy)aniline (0.32 g, 60%, 2.5 mmol scale) following the general procedure B. N-[2-(4-Methoxyphenoxy)phenyl)-N′-(thiazol-2-yl)urea (256 mg, 75%) was prepared from 2-(4-methoxyphenoxy)aniline (215 mg, 1.0 mmol) and 2-aminothiazole (100 mg, 1.0 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-1ebd548f7dba40a5b5422cc4f0841870 |
| Source note | uspto-grants-2009_06 |