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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1031180Generated: October 31, 2026

1-Methylpiperazine → HCID 86745733, compound

https://huagongshe.com/reaction/1031180

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
Reactant2-(2-Chloroethyl)-3,4-dihydro-1,4-dimethyl-1H-[1,3,5]triazepino[3,2-a]benzimidazol-5(2H)-oneHCID 19819759—
ReactantFumaric acid isopropyl alcoholHCID 86745734—
ProductHCID 86745733HCID 86745733—

Reaction Conditions

Temperature60 °C

Reaction Steps

To 20 mL of N-methylpiperazine was added 3.0 g (0.01 mol) of 2-(2-chloroethyl)-3,4-dihydro-1,4-dimethyl-1H-[1,3,5]triazepino[3,2-a]benzimidazol-5(2H)-one. The reaction mixture was heated to 60° C. for 24 hr. The excess amine was removed at 70° C., 0.5 mm Hg. The residual oil was taken up in 60 mL of CH2Cl2 and washed with 2×50 mL of 1N NaOH. The organic layer was dried over Na2SO4, filtered, concentrated by rotary evaporation, and further concentrated at 90° C., 0.5 mm Hg. The residual oil/glass was treated with 2 equivalent of fumaric acid isopropyl alcohol to give 3.4 g of solid. This was recrystallized from isopropyl alcohol to give 3.0 g (51%) off-white analytically pure material, mp 171°-79° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05109013
Source datasetuspto-grants-1992_04
ORD IDord-8d2efe37b54f41a68976cb4e18bc5e84
Source noteuspto-grants-1992_04