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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1706995Generated: November 1, 2026

1-Methylpiperazine → HCID 53680343, compound

https://huagongshe.com/reaction/1706995

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
ReactantHCID 54482160HCID 54482160—
SolventMethanolHCID 887—
ProductHCID 53680343HCID 53680343—

Reaction Steps

A mixture of 8.0 g (0.015 mole) of 1-[2-(o-chlorobenzoyl)-4-chlorophenyl]-5-(iodomethyl)-1H-1,2,4-triazole-3-carboxylic acid methyl ester [see Example 13 b)] and 3.3 ml of 1-methyl-piperazine in 160 ml of methanol is stirred for 16 hours at 40°. The reaction solution is then concentrated in vacuo; water is added to the residue and extraction is performed twice with methylene chloride. The organic phase is washed twice with icewater, and extraction is then performed twice with 2N hydrochloric acid solution. To the aqueous acidified extracts there are added ice and sufficient 5N sodium hydroxide solution to bring the pH-value to 10. The base that has precipitated is taken up in ether. The organic phase is washed twice with saturated sodium chloride solution; it is afterwards dried over sodium sulphate and concentrated in vacuo to dryness. There is obtained 1-[2-(o-chlorobenzoyl)-4-chlorophenyl]-5-[(4-methyl-1-piperazinyl)-methyl]-1H-1,2,4-triazole-3-carboxylic acid methyl ester as solidified foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04209516
Source datasetuspto-grants-1980_06
ORD IDord-f7d1c0ed6eef41089d4b2b38cd09cf81
Source noteuspto-grants-1980_06