Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1954782Generated: October 26, 2026

Diethyl Ether → (R)-N-[8-(4-methylpiperazin-1-yl)-1,2,3,4-tetrahydro-2-naphthyl]methanesulfonamide

https://huagongshe.com/reaction/1954782

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant(R)-2-amino-8-(4-methylpiperazin-1-yl)-1,2,3,4-tetrahydronaphthaleneHCID 53960413—
SolventPyridineHCID 1049—
Product(R)-N-[8-(4-methylpiperazin-1-yl)-1,2,3,4-tetrahydro-2-naphthyl]methanesulfonamideHCID 5453369363.1%

Reaction Steps

To an ice-cooled solution of (R)-2-amino-8-(4-methylpiperazin-1-yl)-1,2,3,4-tetrahydronaphthalene (120 mg, 0.49 mmol) and triethylamine (0.50 mL, 3.6 mmol) in pyridine (15 mL) was added dropwise methanesulfonyl chloride (62 μL, 0.54 mmol). After the addition the reaction was allowed to stir at ambient temperature for 1 h. The solvent was evaporated in vacuo and the residue was purified on a silica gel column using chloroform/methanol/concentrated ammonium hydroxide (95:5:0.5) as the eluent. This gave, after crystalization from diethyl ether, 100 mg (63% yield) of the title compound as white crystals: mp 135-137° C.; [α]21D +22° (c 0.50, chloroform); EIMS (70 eV) m/z (relative intensity) 323 (59, M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06124283
Source datasetuspto-grants-2000_09
ORD IDord-3910b815e51d42ec8e6967b6175ce416
Source noteuspto-grants-2000_09