HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(Difluoromethoxy)benzenesulfonyl chloride → HCID 67094709, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(Difluoromethoxy)benzenesulfonyl chloride | HCID 2778226 | — |
| Reactant | HCID 67094969 | HCID 67094969 | — |
| Product | HCID 67094709 | HCID 67094709 | — |
Reaction Steps
The compound was prepared by analogy to Example 7, starting from commercially available 1-bromo-3-fluoro-2-methoxy-5-nitrobenzene, which was reacted with tert.butyloxycarbonyl-piperazine by analogy to preparation example 3.1 top yield 1-(N-boc-piperazin-4-yl)-3-fluoro-2-methoxy-5-nitrobenzene. Reduction of the nitro group to the corresponding aniline by analogy to preparation example 3.2, subsequent coupling with commercially available 3-difluoromethoxybenzenesulfonylchloride by analogy to preparation example 1.4, and final deprotection of the tert.-butoxycarbonyl group 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-903c7b67203f499e8fc5c361e71b3476 |
| Source note | uspto-grants-2010_09 |