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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 916563Generated: October 28, 2026

Water → Acetamide, N-[4-[(4-methyl-1-piperazinyl)sulfonyl]phenyl]-

https://huagongshe.com/reaction/916563

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantN-Acetylsulfanilyl chlorideHCID 8481—
Reactant1-MethylpiperazineHCID 53167—
SolventDichloromethaneHCID 6344—
ProductAcetamide, N-[4-[(4-methyl-1-piperazinyl)sulfonyl]phenyl]-HCID 76449441%

Reaction Steps

A suspension of 4-acetylaminobenzene sulfonyl chloride (4.5 mmol) in anhydrous CH2Cl2 at room temperature is treated with 1-methyl piperazine (4.5 mmol) and triethylamine (4.5 mmol). The reaction mixture was stirred at room temperature for 1 hour, water was added, and the product extracted with additional CH2Cl2. The combined organic extracts were dried (Na2SO4), filtered, and evaporated under reduced pressure, affording the desired N-[4-(4-methylpiperazine-1-sulfonyl)phenyl]acetamide. Mp: 184° C.; Yield 41%; 1H NMR (DMSO d6): δ 2.09 (s, 3H), 2.15 (s, 3H), 2.40 (m, 4H), 2.85 (m, 4H), 7.63-7.68 (d,2H, J=10 Hz), 7.80-7.84 (d, 2H, J=8 Hz), 10.41 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07271171B2
Source datasetuspto-grants-2007_09
ORD IDord-d577b767647e468c891e2fe101832c28
Source noteuspto-grants-2007_09