HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminothiazole → 1-(Cyclopentyloxy)-2-nitrobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminothiazole | HCID 2155 | — |
| Reactant | Cyclopentanol | HCID 7298 | — |
| Reactant | 1-Fluoro-2-nitrobenzene | HCID 73895 | — |
| Reactant | 2-(Cyclopentyloxy)aniline | HCID 6485398 | — |
| Product | 1-(Cyclopentyloxy)-2-nitrobenzene | HCID 22164473 | 80% |
| Product | N-(2-Cyclopentyloxyphenyl)-N'-(thiazol-2-yl)urea | HCID 59732940 | 70% |
Reaction Steps
2-(Cyclopentyloxy)-1-nitrobenzene (1.04 g, 80%) was prepared from cyclopentanol (0.46 ml, 5.0 mmol) and 1-fluoro-2-nitrobenzene (0.71 g, 5.0 mmol) following the general procedure G. This was reduced to 2-(cyclopentyloxy)aniline (0.30 g, 68%, 2.5 mmol scale) following general procedure B. N-(2-Cyclopentyloxyphenyl)-N′-(thiazol-2-yl)urea (212 mg, 70%) was prepared from 2-(cyclopentyloxy)aniline (177 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 | US07897628B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-c095b2be352943a3b87b1791fcaba1a0 |
| Source note | uspto-grants-2011_03 |