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HRID 80236생성일: 2026년 10월 23일

Potassium Phosphate, Tribasic → 1-Benzothiazol-6-yl-3-(4-dimethoxymethyl-pyridin-3-yl)-imidazolidin-2-one

https://huagongshe.com/ko/reaction/80236

반응식

참여 물질

역할이름HCID투입량
반응물Potassium Phosphate, TribasicHCID 62657—
반응물1-N,2-N-dimethylcyclohexane-1,2-diamineHCID 551074—
반응물3-Bromo-4-(dimethoxymethyl)pyridineHCID 20715145—
반응물1-Benzothiazol-6-yl-imidazolidin-2-oneHCID 66678554—
촉매Copper iodideHCID 83717—
용매MethanolHCID 887—
용매ChloroformHCID 6212—
용매1,4-DioxaneHCID 31275—
생성물1-Benzothiazol-6-yl-3-(4-dimethoxymethyl-pyridin-3-yl)-imidazolidin-2-oneHCID 4987245252.9%

반응 단계

Using the same reaction conditions and work up as described in Example 1, step-3,1-benzothiazol-6-yl-imidazolidin-2-one (I-84b: 515 mg, 2.35 mmol) was refluxed with 3-bromo-4-dimethoxymethyl-pyridine (600 mg, 2.584 mmol), copper iodide (44.7 mg, 0.2312 mmol), N,N′-dimethyl-cyclohexane-1,2-diamine (80.8 mg, 0.7405 mmol), potassium phosphate (1.4 g, 7.046 mmol) and 1,4-dioxane (20 mL) at 110° C. for 12 hours to afford the crude product. The reaction was monitored by TLC (10% MeOH in chloroform). Purification by column chromatography on silica gel (2% methanol in chloroform) afforded 460 mg of the product (52.9% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호USRE045173E1
출처 데이터셋uspto-grants-2014_09
ORD IDord-9528f764c4114816a73e1d2b7b3500d0
출처 메모uspto-grants-2014_09