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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 247471생성일: 2026년 10월 26일

Sodium Iodide → HCID 13911228, 화합물

https://huagongshe.com/reaction/247471

반응식

참여 물질

역할이름HCID투입량
반응물Sodium IodideHCID 5238—
반응물Sodium HydroxideHCID 14798—
반응물Sodium BicarbonateHCID 516892—
반응물N-(2-Methoxyphenyl)piperazine hydrochlorideHCID 9899402—
반응물HCID 13911227HCID 13911227—
용매TetrahydrofuranHCID 8028—
생성물HCID 13911228HCID 1391122850.2%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04707550
출처 데이터셋uspto-grants-1987_11
ORD IDord-cd4056b9d58547288e68a0d57de1a1fd
출처 메모uspto-grants-1987_11