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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 247471Generated: October 25, 2026

Sodium Iodide → HCID 13911228, compound

https://huagongshe.com/reaction/247471

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantSodium HydroxideHCID 14798—
ReactantSodium BicarbonateHCID 516892—
ReactantN-(2-Methoxyphenyl)piperazine hydrochlorideHCID 9899402—
ReactantHCID 13911227HCID 13911227—
SolventTetrahydrofuranHCID 8028—
ProductHCID 13911228HCID 1391122850.2%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04707550
Source datasetuspto-grants-1987_11
ORD IDord-cd4056b9d58547288e68a0d57de1a1fd
Source noteuspto-grants-1987_11