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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710612Generated: November 3, 2026

3-(Difluoromethoxy)benzenesulfonyl chloride → HCID 67094709, compound

https://huagongshe.com/reaction/1710612

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Difluoromethoxy)benzenesulfonyl chlorideHCID 2778226—
ReactantHCID 67094969HCID 67094969—
ProductHCID 67094709HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790727B2
Source datasetuspto-grants-2010_09
ORD IDord-903c7b67203f499e8fc5c361e71b3476
Source noteuspto-grants-2010_09