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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1198908Generated: October 29, 2026

Aminoethylpiperazine → 2-Chloro-4-(2,3,4,5-tetrahydro-5-methyl-3-oxo-1,2,4-triazin-6-yl)phenoxy-N-[2-(1-piperazinyl)ethyl]acetamide

https://huagongshe.com/reaction/1198908

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAminoethylpiperazineHCID 8795—
ReactantEthyl alpha-[2-chloro-4-(2,3,4,5-tetrahydro-5-methyl-3-oxo-1,2,4-triazin-6-yl)phenoxy]acetateHCID 14370696—
SolventEthanolHCID 702—
Product2-Chloro-4-(2,3,4,5-tetrahydro-5-methyl-3-oxo-1,2,4-triazin-6-yl)phenoxy-N-[2-(1-piperazinyl)ethyl]acetamideHCID 1437070068.5%

Reaction Steps

4.0 g of ethyl α-[2-chloro-4-(2,3,4,5-tetrahydro-5-methyl-3-oxo-1,2,4-triazin-6-yl)phenoxy]acetate (prepared as described in Example 5) and 1.59 g of N-(2-aminoethyl)piperazine were added to 50 ml of ethanol, and the mixture was heated under reflux for 60 hours. The mixture was then cooled, after which the crystals which precipitated were collected by filtration and then recrystallized from ethanol to give 3.44 g of the title compound as pale yellow prisms melting at 208°-210° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04898862
Source datasetuspto-grants-1990_02
ORD IDord-5605edfe49b14265bdec99415c7d4293
Source noteuspto-grants-1990_02