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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1783406Generated: November 1, 2026

Benzoyl chloride → HCID 68623959, compound

https://huagongshe.com/reaction/1783406

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
ReactantHCID 68623756HCID 68623756—
SolventDichloromethaneHCID 6344—
ProductHCID 68623959HCID 6862395959.7%

Reaction Steps

4-Chloro-N-((R)-5,5-difluoro-2-oxo-azepan-3-yl)-N-piperidin-4-ylmethyl-benzenesulfonamide (0.04 g, 0.09 mmol) and triethylamine (19 mg, 0.18 mmol) were dissolved in dichloromethane (1.5 ml). Then benzoyl chloride (0.018 g, 0.13 mmol) was added and the mixture was stirred overnight at room temperature. The reaction mixture was partitioned between aqueous sodium bicarbonate solution and ethyl acetate. The organic layer was dried (MgSO4) and concentrated under reduced pressure. The residue was purified over silica gel (heptane/ethyl acetate 1:1) to yield 29 mg (58%) of the title compound;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07501406B2
Source datasetuspto-grants-2009_03
ORD IDord-9fca5523fdbe41458e37906910fc45ca
Source noteuspto-grants-2009_03