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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 529678생성일: 2026년 10월 25일

1,4-Dioxane → 4-((2-Chloro-5-(2-methylbenzo[d]oxazol-6-yl)-7-((2-(trimethylsilyl)ethoxy)-methyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl)oxy)-1-methylcyclohexanol

https://huagongshe.com/reaction/529678

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참여 물질

역할이름HCID투입량
반응물1,4-DioxaneHCID 31275—
반응물Tripotassium phosphate trihydrateHCID 18407952—
반응물2-Methyl-6-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1,3-benzoxazoleHCID 70975061—
반응물4-((2-Chloro-5-iodo-7-((2-(trimethylsilyl)ethoxy)methyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl)oxy)-1-methylcyclohexanolHCID 86726445—
용매WaterHCID 962—
생성물4-((2-Chloro-5-(2-methylbenzo[d]oxazol-6-yl)-7-((2-(trimethylsilyl)ethoxy)-methyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl)oxy)-1-methylcyclohexanolHCID 8672644695%

반응 조건

온도70 °C

반응 단계

To a degassed mixture of 4-((2-chloro-5-iodo-7-((2-(trimethylsilyl)ethoxy)methyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl)oxy)-1-methylcyclohexanol (1 equiv), 2-methyl-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzo[d]oxazole (1.2 equiv) and tripotassium phosphate trihydrate (3 equiv) in a 9:1 mixture of 1,4-dioxane and water (0.18 M) was added palladium 1,1-bis(diphenylphosphion)ferrocene dichloride (0.1 equiv). The reaction mixture was stirred at 70° C. for 3 h. After the reaction was completed, the reaction mixture was cooled to room temperature and concentrated. The residue was purified by silica gel chromatography (0-2% DCM in methanol) to afford the title compound (95% yield) as a red oil. MS (ESI) m/z 543.2 [M+1]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09346812B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-f59ac7e8d2874b1198d3d4ee41b147b8
출처 메모uspto-grants-2016_05