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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 641521생성일: 2026년 10월 26일

Pyrazole → 3-Cyclobutyl-7-{[5-(1H-pyrazol-1-yl)-2-pyridinyl]oxy}-2,3,4,5-tetrahydro-1H-3-benzazepine

https://huagongshe.com/reaction/641521

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참여 물질

역할이름HCID투입량
반응물PyrazoleHCID 1048—
반응물1,10-PhenanthrolineHCID 1318—
반응물Cesium carbonateHCID 10796—
반응물1H-3-Benzazepine, 3-cyclobutyl-2,3,4,5-tetrahydro-7-[(5-iodo-2-pyridinyl)oxy]-HCID 57440294—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매Ethyl AcetateHCID 8857—
용매1,4-DioxaneHCID 31275—
생성물3-Cyclobutyl-7-{[5-(1H-pyrazol-1-yl)-2-pyridinyl]oxy}-2,3,4,5-tetrahydro-1H-3-benzazepineHCID 10473695—

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온도180 °C

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A mixture of 3-cyclobutyl-7-[(5-iodo-2-pyridinyl)oxy]-2,3,4,5-tetrahydro-1H-3-benzazepine (E207) (294 mg, 0.7 mmol), pyrazole (58 mg, 0.84 mmol), cesium carbonate (479 mg, 1.5 mmol), copper (I) iodide (7 mg, 0.04 mmol) and 1.10 phenanthroline (13 mg, 0.07 mmol) in dioxane (2 ml) were heated in a microwave reactor at 180° C. for 20 minutes. The reaction mixture was diluted with ethyl acetate and washed with a saturated solution of ammonium chloride, water, brine and dried (magnesium sulfate). The organic layer was filtered, concentrated in vacuo and the resulting residue was purified by column chromatography eluting with a mixture of 0.880 ammonia:methanol:dichloromethane (0.5:4.5:95) to afford the title compound (E221); MS (ES+) m/e 361 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07696193B2
출처 데이터셋uspto-grants-2010_04
ORD IDord-90270f2a441f47d98c7f1ad60d050698
출처 메모uspto-grants-2010_04