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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 544946생성일: 2026년 10월 25일

Potassium Acetate → 5-(5-(Cyclopropylcarbamoyl)-2-methylphenylcarbamoyl)thiophen-2-ylboronic acid

https://huagongshe.com/reaction/544946

반응식

참여 물질

역할이름HCID투입량
반응물Potassium AcetateHCID 517044—
반응물Bis(pinacolato)diboraneHCID 2733548—
반응물(2-Chlorophenyl)-N-(5-(cyclopropylcarbamoyl)-2-methylphenyl)thiophene-2-carboxamideHCID 67148792—
용매DimethylformamideHCID 6228—
생성물5-(5-(Cyclopropylcarbamoyl)-2-methylphenylcarbamoyl)thiophen-2-ylboronic acidHCID 59761503178.3%

반응 조건

온도90 °C

반응 단계

A solution of 1.0 g (2.64 mmol) of 5-bromo-N-(5-(cyclopropylcarbamoyl)-2-methylphenyl)thiophene-2-carboxamide (Example 136, Step B), bis(pinacolato)diborane (1.0 g, 3.95 mmol) and KOAc (1.30 g, 13.2 mmol) in DMF (15 mL) was purged with argon and Pd(dppf)2Cl2/CH2Cl2 complex (65 mg, 0.08 mmol) was added followed by heating at 90° C. for 16 h. After cooling to rt, the mixture was partitioned between EtOAc (250 mL) and water (50 mL) and the layers were separated. The organic portion was washed with additional water, then brine, then dried over anhyd Na2SO4, filtered, and concentrated under vacuum to afford 1.62 g of a brown semi-solid as the crude product mixture. This material was triturated with EtOAc and filtered to afford 626 mg of the compound a containing ˜10% of the boronate ester. This material was used as is without any further purification. HPLC Ret time=2.36 min. LCMS [M+H]+ 345.2.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07935696B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-135ecc26917e4d76af946caa32bbb78a
출처 메모uspto-grants-2011_05