HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromo-4-nitrophenol → 2-Bromo-1-(difluoromethoxy)-4-nitrobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromo-4-nitrophenol | HCID 22109 | — |
| Reactant | 2-Chloro-2,2-difluoroacetophenone | HCID 238296 | — |
| Product | 2-Bromo-1-(difluoromethoxy)-4-nitrobenzene | HCID 13314704 | — |
Reaction Steps
The compound was prepared starting from commercially available 2-bromo-4-nitrophenol, which was reacted with 2-chloro-2,2-difluoroacetophenone (J. Hu et al., J. Org. Chem., 2006, 71, 9845) to yield 2-bromo-1-difluoromethoxy-4-nitro-benzene. Subsequent Buchwald-Hartwig coupling of 2-bromo-1-difluoromethoxy-4-nitro-benzene with tert.butyloxycarbonyl-piperazine by analogy to preparation example 3.1, reduction of the nitro group to the corresponding aniline by analogy to preparation example 3.2, subsequent coupling with commercially available 2-difluoromethoxybenzene-sulfonylchloride by analogy to preparation example 1.4, and final deprotection under acidic conditions by analogy to example 1 yielded the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07790727B2 |
| Source dataset | uspto-grants-2010_09 |
| ORD ID | ord-300dfa31e44440ff94595fdfd52190d2 |
| Source note | uspto-grants-2010_09 |