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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 726703Generated: November 3, 2026

Pyridine → HCID 19706883, compound

https://huagongshe.com/reaction/726703

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantHCID 10567395HCID 10567395—
Reactant[1,1'-Biphenyl]-2-carbonyl chlorideHCID 12563768—
SolventDichloromethaneHCID 6344—
ProductHCID 19706883HCID 19706883—

Reaction Steps

1-(4-Aminobenzoyl)-4,4-difluoro-2,3,4,5-tetrahydro-1H-1-benzazepin-5-one (200 mg) and 5 ml of pyridine were dissolved in 10 ml of methylene chloride, and 10 ml of a methylene chloride solution containing the o-phenylbenzoic acid chloride obtained above was added dropwise under ice-cooling. After 1 hour of stirring at room temperature, the solvent was evaporated under a reduced pressure, and the thus obtained residue was dissolved in ethyl acetate and washed with saturated sodium carbonate aqueous solution, 1N hydrochloric acid aqueous solution and saturated sodium chloride aqueous solution in that order. After drying on anhydrous magnesium sulfate and subsequent evaporation of the solvent under a reduced pressure, the resulting residue was applied to column chromatography, which was eluted with a mixed solvent of ethyl acetate and hexane (2:3, v/v) to obtain 283 mg of 4,4-difluoro-1-[4-(2-phenylbenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-1-benzazepin-5-one. This product was recrystallized from ethyl acetate-hexane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05710150
Source datasetuspto-grants-1998_01
ORD IDord-5ac8d8c2056749febb899f3fe0b2f782
Source noteuspto-grants-1998_01