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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 247471Erstellt: 25. Oktober 2026

Sodium Iodide → HCID 13911228, Verbindung

https://huagongshe.com/reaction/247471

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium IodideHCID 5238—
EduktSodium HydroxideHCID 14798—
EduktSodium BicarbonateHCID 516892—
EduktN-(2-Methoxyphenyl)piperazine hydrochlorideHCID 9899402—
EduktHCID 13911227HCID 13911227—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 13911228HCID 1391122850,2%

Reaktionsschritte

A 500 ml tetrahydrofuran mixture containing 13.1 g (50 mmol) of N-(3-carbomethoxythien-4-yl)-N'-(2-chloroethyl)urea from (a), 35 g (150 mmol) of 1-(2-methoxyphenyl)piperazine hydrochloride, 21 g (250 mmol) of sodium bicarbonate and 3.75 g (25 mmol) of sodium iodide was heated to reflux under nitrogen for 4 days. The tetrahydrofuran was removed in vacuo and the residue was partitioned between H2O and CH2Cl2. The CH2Cl2 extracts were dried over MgSO4 and evaporated to dryness. This residue which contained the title compound of Example 2 was dissolved in 300 ml of methanol and treated with 4.5 g (56 mmol) of 50% NaOH. After the solution had been stirred at room temperature for 16 hours, the resulting precipitate was collected by filtration to afford 9.7 g of the title compound. The filtrate was purified by flash silica gel chromatography using 1-5% MeOH in CH2Cl2. There was obtained an additional 3.4 g of the title compound (13.1 g total, 68%) which was converted to its hydrochloride salt with isopropanolic hydrogen chloride, 9.1 g, mp 273°-275° C. (dec).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04707550
Quelldatensatzuspto-grants-1987_11
ORD IDord-cd4056b9d58547288e68a0d57de1a1fd
Quellennotizuspto-grants-1987_11