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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1408433생성일: 2026년 10월 25일

Potassium Carbonate → methyl N-[[2-chloro-5-(1-spiro[2H-1-benzopyran-3(4H), 2'-[1,3]dioxolan]-6-yl-1H-pyrazol-3-yl)phenyl]methyl]carbamate

https://huagongshe.com/reaction/1408433

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참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물trans-N,N'-dimethyl-1,2-cyclohexanediamineHCID 2733821—
반응물6-Bromospiro[2H-1-benzopyran-3(4H),2'-[1,3]dioxolane]HCID 67151224—
반응물HCID 178502067HCID 178502067—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매1,4-DioxaneHCID 31275—
용매Chloroform methanolHCID 21584188—
생성물methyl N-[[2-chloro-5-(1-spiro[2H-1-benzopyran-3(4H), 2'-[1,3]dioxolan]-6-yl-1H-pyrazol-3-yl)phenyl]methyl]carbamateHCID 6715120218%

반응 조건

온도100 °C

반응 단계

To a solution of methyl N-[[2-chloro-5-(1H-pyrazol-3-yl)phenyl]-methyl]carbamate (i.e. the product of Example 8, Step B) (400 mg, 1.50 mmol) in dioxane (16 mL) was added trans-N,N′-dimethylcyclohexane-1,2-diamine (0.30 mmol, 43 mg) under a nitrogen atmosphere. Copper (I) iodide (57 mg, 0.30 mmol) and potassium carbonate (1.24 g, 9.05 mmol) were added to the reaction mixture. 6-Bromospiro[2H-1-benzopyran-3(4H),2′-[1,3]dioxolane] (614 mg, 2.26 mmol) was added last and the reaction mixture was heated at 100° C. under a nitrogen atmosphere overnight. After TLC analysis (10% MeOH/CHCl3) shows 80% conversion of starting material, the reaction mixture was concentrated under vacuum. The resultant crude residue was purified on a silica gel column with 1% MeOH/CHCl3 as eluent to give the title compound, a compound of the present invention, (120 mg, 18% yield) as a solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08921360B2
출처 데이터셋uspto-grants-2014_12
ORD IDord-ce243556125d44748366bd2ac656a2b1
출처 메모uspto-grants-2014_12