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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1865956Generated: October 25, 2026

3,5-Difluorobenzoyl chloride → 5-Bromo-1'-[{6-chloro-1-(3,5-difluorobenzoyl)-1H-indol-3-yl]carbonyl}-3H-spiro[2-benzofuran-1,4'-piperidin]-3-one

https://huagongshe.com/reaction/1865956

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-Difluorobenzoyl chlorideHCID 145600—
Reactant5-bromo-1'-[(6-chloro-1H-indol-3-yl)carbonyl]-3H-spiro[2-benzofuran-1,4'-piperidin]-3-oneHCID 59657619—
Product5-Bromo-1'-[{6-chloro-1-(3,5-difluorobenzoyl)-1H-indol-3-yl]carbonyl}-3H-spiro[2-benzofuran-1,4'-piperidin]-3-oneHCID 59657645—

Reaction Steps

Following the general procedure VII as described above, the acylation of 5-bromo-1′-[(6-chloro-1H-indol-3-yl)carbonyl]-3H-spiro[2-benzofuran-1,4′-piperidin]-3-one with commercially available 3,5-difluorobenzoyl chloride gave the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07629353B2
Source datasetuspto-grants-2009_12
ORD IDord-4aae3ad97e724b43a9619c57de8401c2
Source noteuspto-grants-2009_12