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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35561Generated: October 29, 2026

1-Methylpiperazine → HCID 23035201, compound

https://huagongshe.com/reaction/35561

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
Reactant2,6-dichloro-alpha-(4-chlorophenyl)-4(4,5-dihydro-3,5-dioxo-1,2,4-triazin-2(3H)-yl)benzeneacetylchlorideHCID 22557320—
SolventTetrahydrofuranHCID 8028—
ProductHCID 23035201HCID 2303520162.8%

Reaction Steps

To a stirred mixture of 10 parts of 1-methylpiperazine in 45 parts of tetrahydrofuran was added dropwise a solution of 6.7 parts of 2,6-dichloro-α-(4-chlorophenyl)-4-(4,5-dihydro-3,5-dioxo-1,2,4-triazin-2(3H)-yl)benzeneacetyl chloride in 45 parts of tetrahydrofuran during a period of 5 minutes. Upon complete addition, stirring was continued for 2 hours at room temperature. After evaporation in vacuo, the residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (90:10 by volume) as eluent. The pure fractions were collected and the eluent was evaporated in vacuo. The residue was boiled in acetonitrile. After cooling, the precipitated product was filtered off, washed with 2,2'-oxybispropane and dried, yielding 4.8 parts (62.8%) of 1-[2-(4-chlorophenyl)-2-[2,6-dichloro-4-(4,5-dihydro-3,5-dioxo-1,2,4-triazin-2(3H)-yl)phenyl]acetyl]-4-methylpiperazine; mp. 261.5° C. (intermediate 36).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04767760
Source datasetuspto-grants-1988_08
ORD IDord-e1c86fddfdad44c4888e4de28be5b65c
Source noteuspto-grants-1988_08