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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2086271Generated: October 29, 2026

Hydrochloric Acid → 1-Amino-4-(6-chloronaphthalene-2-sulfonyl)-2-piperazinone

https://huagongshe.com/reaction/2086271

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantSodium BicarbonateHCID 516892—
Reactant1-(Tert-butoxycarbonylamino)-4-(6-chloronaphthalene-2-sulfonyl)-2-piperazinoneHCID 22727035—
SolventEthyl AcetateHCID 8857—
Product1-Amino-4-(6-chloronaphthalene-2-sulfonyl)-2-piperazinoneHCID 22727083—

Reaction Steps

1-(tert-Butoxycarbonylamino)-4-(6-chloronaphthalene-2-sulfonyl)-2-piperazinone (575 mg) was combined with methanol (4 ml) and a 4N solution of hydrochloric-acid in ethyl acetate (4 ml) and stirred at room temperature for 30 minutes. The reaction mixture was concentrated and the residue obtained was combined with aqueous sodium bicarbonate, extracted with dichloromethane, dried and concentrated to obtain 1-amino-4-(6-chloronaphthalene-2-sulfonyl)-2-piperazinone as a colorless solid. A solution of the resultant 1-amino-4-(6-chloronaphthalene-2-sulfonyl)-2-piperazinone and 1-(4-pyridyl)-4-piperidone (237 mg) in ethanol (30 ml) was dehydrated using a Soxlet extractor packed with molecular sieves 4A while refluxing for 24 hours. The reaction mixture was concentrated and the residue was purified by a column chromatography (dichloromethane: 10% aqueous ammonia-containing methanol=20:1) and crystallized from ether to obtain the title compound (265 mg) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06723722B1
Source datasetuspto-grants-2004_04
ORD IDord-550b6c9df9a94facb9fbeff0ebe20bbf
Source noteuspto-grants-2004_04