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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1054424생성일: 2026년 10월 27일

1-Benzyl-1H-pyrazole-4-boronic acid → 5-(1-Benzyl-1H-pyrazol-4-yl)-[1,2,4]triazolo[1,5-c]pyrimidin-2-ylamine

https://huagongshe.com/reaction/1054424

반응식

참여 물질

역할이름HCID투입량
반응물1-Benzyl-1H-pyrazole-4-boronic acidHCID 3352881—
반응물5-Methylsulfanyl-[1,2,4]triazolo[1,5-c]pyrimidin-2-ylamineHCID 59589529—
촉매Cuprous 2-thiophenecarboxylateHCID 11194830—
촉매HCID 178418397HCID 178418397—
용매TetrahydrofuranHCID 8028—
생성물5-(1-Benzyl-1H-pyrazol-4-yl)-[1,2,4]triazolo[1,5-c]pyrimidin-2-ylamineHCID 59589583—

반응 조건

온도130 °C

반응 단계

A microwave vial containing 5-methylsulfanyl-[1,2,4]triazolo[1,5-c]pyrimidin-2-ylamine (0.05 g, 0.276 mmol), 1-benzyl-1H-pyrazole-4-boronic acid (123 mg, 0.607 mmol), copper(I)thiophene carboxylate (116 mg, 0.607 mmol) and tetrakis(triphenylphosphine)palladium (33 mg, 0.028 mmol) in THF (1.2 mL) was heated under microwave irradiation (130° C., 15 min). The reaction mixture was filtered through celite and the cake washed with dichloromethane. The filtrate was washed with water followed by brine, dried over magnesium sulfate and concentrated under vacuum. Trituration with diethyl ether provided a yellow solid that did not require further purification. Yield: 0.05 g, 63%; LCMS method: 2, RT: 3.18 min, MI: 292 [M+1].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09394301B2
출처 데이터셋uspto-grants-2016_07
ORD IDord-913f62aa73c046fca213e8f2cf00bfe2
출처 메모uspto-grants-2016_07