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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2284296Generated: October 30, 2026

Pyridine → HCID 67112407, compound

https://huagongshe.com/reaction/2284296

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantCyclopropanecarbonyl chlorideHCID 77637—
ReactantHCID 67112462HCID 67112462—
SolventDichloromethaneHCID 6344—
ProductHCID 67112407HCID 6711240790%

Reaction Steps

A solution of cyclopropanecarbonyl chloride (Aldrich, 448 mg, 4.31 mmol) in 5 mL of methylene chloride was slowly added over 5 minutes to N-(4-(4-aminobenzoyl)phenyl)-4-fluorobenzamide (1.2 g, 3.59 mmol) in 20 mL of methylene chloride containing 3 mL of pyridine. The reaction was stirred at room temperature for 12 h then quenched with 40 mL of water. The layers were separated and the aqueous layer was extracted with ethyl acetate (2×50 mL). The combined organics were washed with 0.5 N HCl (100 mL), brine (100 mL), dried over sodium sulphate, and filtered. Concentration of the organics provided N-(4-(4-(cyclopropanecarboxamido)benzoyl)phenyl)-4-fluorobenzamide (1.3 g, 3.23 mmol) as a tan solid which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09144557B2
Source datasetuspto-grants-2015_09
ORD IDord-6aeed0e743744ba299e8b8afc85c900c
Source noteuspto-grants-2015_09