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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 863822Generated: October 30, 2026

Methyl iodide → HCID 19420471, compound

https://huagongshe.com/reaction/863822

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantHexahydro-1,4-diazepineHCID 68163—
SolventEthanolHCID 702—
ProductHCID 19420471HCID 19420471—

Reaction Conditions

Temperature95 °C

Reaction Steps

To a solution of homopiperazine (5 g, 50 mmol) in 10 mL of ethanol added a solution of methyl iodide (0.62 mL, 10 mmol) in 5 mL of ethanol in a sealed tube. It was gently stirred at 95° C. for 5 hours. The resulting white precipitate was filtered, washed with a small mount of cold ethanol, and the filtrate was concentrated in vacuo to yield 1-methyl homopiperazine hydroiodide. MS m/z M+H=115. The obtained 1-methylhomopiperazine hydroiodide is convened into free base according to the procedure describing in Example 25. Following the procedure of Example 6, but replacing 1-benzylpiperazine with 1-methyl homopiperazine, provides the desired compound. The product of Example 3 (2.1 g, 2.03 mmol), 1-methylhomopiperazine (700 mg, 6.09 mmol), and triethylamine (0.85 mL, 6.09 mmol) in 10 mL of methylene chloride are used. The reaction is carried out at 45° C. for 15 hours. Semi-pure compound is isolated from silica gel column chromatography.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05561140
Source datasetuspto-grants-1996_10
ORD IDord-3c921b4aec1243baaf38a5ef26096c23
Source noteuspto-grants-1996_10