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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1090351Generated: November 2, 2026

Triethylamine → 1-(Methanesulfonyl)-4-methylpiperazine

https://huagongshe.com/reaction/1090351

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant1-MethylpiperazineHCID 53167—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product1-(Methanesulfonyl)-4-methylpiperazineHCID 817770—

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of N-methylpiperazine (3.0 g, 29.9 mmol), triethylamine (3.6 g, 35.9 mmol) and methanesulfonyl chloride (Compound 19, 4.11 g, 35.9 mmol) in tetrahydrofuran (20 ml) was stirred at 0° C. for 2 hours. The mixture was filtered and the filtrate was evaporated to dryness to give a solid. The solid was redissolved in ethyl acetate and washed with water. Evaporation of the dried (magnesium sulfate) organic phase gave the title sulfonamide. 1HNMR(CDCl3): 2.35 (s, 3H), 2.53 (t, 4H, J=5.0 Hz), 2.79 (s, 3H) and 3.27 (t, 4H, J=5.0 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05081261
Source datasetuspto-grants-1992_01
ORD IDord-64a6c1fc458b4e65b8b1b9e06ea89865
Source noteuspto-grants-1992_01