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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 15994생성일: 2026년 10월 26일

Nitrogen → 1-(2,3-dihydro-benzofuran-5-ylmethyl)-6-(1-methyl-1H-pyrazol-4-yl)-1H-[1,2,3]triazolo[4,5-b]pyrazine

https://huagongshe.com/reaction/15994

반응식

참여 물질

역할이름HCID투입량
반응물NitrogenHCID 947—
반응물Sodium CarbonateHCID 10340—
반응물1-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazoleHCID 2773987—
반응물6-bromo-1-(2,3-dihydro-benzofuran-5-ylmethyl)-1H-[1,2,3]triazolo[4,5-b]pyrazineHCID 59341844—
촉매HCID 178418476HCID 178418476—
용매Water 1,2-dimethoxyethaneHCID 18180031—
생성물1-(2,3-dihydro-benzofuran-5-ylmethyl)-6-(1-methyl-1H-pyrazol-4-yl)-1H-[1,2,3]triazolo[4,5-b]pyrazineHCID 5934179024%

반응 조건

온도80 °C

반응 단계

To a solution of 6-bromo-1-(2,3-dihydro-benzofuran-5-ylmethyl)-1H-[1,2,3]triazolo[4,5-b]pyrazine (50 mg, 0.15 mmol), 1-methyl-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-1H-pyrazole (34 mg, 0.165 mmol), and sodium carbonate (48 mg, 0.45 mmol) in DME/water (4 mL/1 mL) degassed with N2 was added Pd(PPh3)2Cl2 (5 mg, 0.008 mmol). The reaction solution was degassed with N2 again and stirred for 16 hours at 80° C. The reaction mixture was filtered through celite, concentrated, and purified with a reverse-phased preparative HPLC eluting with acetonitrile-water having 0.1% acetic acid to give 1-(2,3-dihydro-benzofuran-5-ylmethyl)-6-(1-methyl-1H-pyrazol-4-yl)-1H-[1,2,3]triazolo[4,5-b]pyrazine (12 mg, 24% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732604B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-f62c3f5f9af44c268194a6c5eef725fd
출처 메모uspto-grants-2010_06