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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1165856Generated: November 1, 2026

Benzoyl chloride → HCID 19860973, compound

https://huagongshe.com/reaction/1165856

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantHCID 23035205HCID 23035205—
SolventPyridineHCID 1049—
ProductHCID 19860973HCID 1986097320.2%

Reaction Steps

To a stirred mixture of 3 parts of 2,6-dichloro-α-(4-chlorophenyl)-4-(3,4,5,6-tetrahydro-4-methyl-3,5-dioxo-1,2,4-triazin-2(1H)-yl)-benzeneacetonitrile and 20 parts of pyridine was added dropwise 1.7 parts of benzoyl chloride during a period of 5 minutes at room temperature and under nitrogen atmosphere. Upon complete addition, stirring was continued overnight at room temperature. The reaction mixture was evaporated in vacuo and the residue was stirred in water. The product was extracted with trichloromethane. The extract was dried, filtered and evaporated. The residue was purified twice the column chromatography over silica gel using trichloromethane as eluent. The pure fractions were collected and the eluent was evaporated in vacuo. The residue was crystallized from 8 parts of acetonitrile. The product was filtered off, washed with 2,2'-oxybispropane and dried, yielding 0.8 parts (20.2%) of 1-benzoyl-2-[3,5-dichloro-4-[(4-chlorophenyl)cyanomethyl]phenyl]-1,6-dihydro-4-methyl-1,2,4-triazine-3,5(2H,4H)-dione; mp. 148.4° C. (compound 79).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04912106
Source datasetuspto-grants-1990_03
ORD IDord-9baf3fadbfbb4cf9a68f9aaad15c2513
Source noteuspto-grants-1990_03