HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2,4-Trifluoro-5-nitrobenzene → Ethyl 2-(4,5-difluoro-2-nitroanilino)benzo[b]thiophene-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2,4-Trifluoro-5-nitrobenzene | HCID 75012 | — |
| Reactant | Ethyl 2-amino-1-benzothiophene-3-carboxylate | HCID 699464 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | Ethyl 2-(4,5-difluoro-2-nitroanilino)benzo[b]thiophene-3-carboxylate | HCID 18422335 | — |
Reaction Steps
In the same manner as in Starting Material Synthesis Example 4 and using ethyl 2-aminobenzo[b]thiophene-3-carboxylate, 2,4,5-trifluoronitrobenzene and dimethyl sulfoxide, ethyl 2-(4,5-difluoro-2-nitroanilino)benzo[b]thiophene-3-carboxylate is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06271225B1 |
| Source dataset | uspto-grants-2001_08 |
| ORD ID | ord-21b2f5c3ff864378a970711af5396409 |
| Source note | uspto-grants-2001_08 |