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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1450113Generated: October 28, 2026

Pyridine → HCID 21195030, compound

https://huagongshe.com/reaction/1450113

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantBenzoyl chlorideHCID 7412—
ReactantCni H1894HCID 463010—
ReactantHCID 178465628HCID 178465628—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21195030HCID 21195030—

Reaction Steps

Compound 26, FIG. 7E.26: A solution of 3,5-diacetylaniline (0.885 g) in tetrahydrofuran (10 mL) containing 0.45 mL pyridine was treated with 0.65 mL benzoyl chloride. The mixture was stirred 1 hr, then treated with 1 mL water and stirred 15 min. The mixture was then diluted with 40 mL water and stirred 30 min. Filtration and washing with water and isopropanol gave colorless needles of N-benzoyl-3,5-diacetylaniline, 1.36 g, mp 188°-189° C. A suspension of N-benzoyl-3,5-diacetylaniline (0.844 g) in aq. 87.5% ethanol (8 mL) containing 0.73 g aminoguanidine hydrochloride and a trace of HCl was heated at reflux for 18 hr. Cooling and filtration gave 1.357 g of N-benzoyl-3,5-diacetylaniline bis(amidinohydrazone) dihydrochloride (Compound 26), mp 268°-72° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05599984
Source datasetuspto-grants-1997_02
ORD IDord-e3ffa4c8ea534687897e40f8871d7765
Source noteuspto-grants-1997_02