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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1066348Generated: October 30, 2026

Hydrochloric Acid → HCID 131722606, compound

https://huagongshe.com/reaction/1066348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDimethylformamideHCID 6228—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant1-PentanesulfonamideHCID 10920696—
ReactantHCID 22388054HCID 22388054—
ProductHCID 131722606HCID 131722606—

Reaction Steps

(E)-2-(2-(4-phenylphenyl)ethenyl)pyridine-4-carboxylic acid (277 mg) was dissolved in 2.8 ml of dried dimethylformamide, and 194 mg of carbonyldiimidazole was added thereto. The mixture was stirred at room temperature for 1.5 hours and then stirred at 100° C. for 30 minutes. After being cooled to room temperature, the mixture was mixed with 209 mg of pentanesulfonamide and 210 mg of 1,8-diazabicyclo[5.4.0]undec-7-ene and stirred at 100° C. for 48 hours. The reaction mixture was cooled with ice, and then its pH was adjusted to 5 using 1N hydrochloric acid. The resulting precipitate was collected by filtration and washed with water. The partially purified material thus obtained was further purified by silica-gel thin-layer chromatography (eluent, chloroform:methanol:water=65:25:4) to yield 67 mg of brown powder of (E)-N-(n-pentanesulfonyl)-2-(2-(4-phenylphenyl)ethenyl)pyridine-4-carboxyamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06242474B1
Source datasetuspto-grants-2001_06
ORD IDord-ac09052c541b45ba9226ed5c7c960e9c
Source noteuspto-grants-2001_06