HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminothiazole → 2-(3,5-Dimethylphenylsulfanyl)nitrobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminothiazole | HCID 2155 | — |
| Reactant | 1-Fluoro-2-nitrobenzene | HCID 73895 | — |
| Reactant | 3,5-Dimethylbenzenethiol | HCID 117548 | — |
| Reactant | 2-((3,5-Dimethylphenyl)thio)aniline | HCID 66998967 | — |
| Product | 1-(Thiazol-2-yl)urea | HCID 16781708 | 74% |
| Product | 2-(3,5-Dimethylphenylsulfanyl)nitrobenzene | HCID 66999017 | 78% |
Reaction Steps
2-(3,5-Dimethylphenylsulfanyl)nitrobenzene (1.01 g, 78%) was prepared from 3,5-dimethylthiophenol (0.76 g, 5.5 mmol) and 2-fluoronitrobenzene (0.71 g, 5.0 mmol) following the general procedure A. This compound was reduced to 2-(3,5-dimethylphenylsulfanyl)-aniline (0.64 g, 72%) following the general procedure B. N-[2-3,5-Dimethylphenylsulfanyl)-phenyl]-N′-(thiazol-2-yl)urea (131 mg; 74%) was prepared from 2-(3,5-dimethylphenyl-sulfanyl)aniline (115 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 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-6ab0f95507a24a36a404e275372fe87e |
| Source note | uspto-grants-2009_06 |