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HRID 544946作成日:2026年10月26日

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

https://huagongshe.com/reaction/544946

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium AcetateHCID 517044—
反応物Bis(pinacolato)diboraneHCID 2733548—
反応物(2-Chlorophenyl)-N-(5-(cyclopropylcarbamoyl)-2-methylphenyl)thiophene-2-carboxamideHCID 67148792—
溶媒DimethylformamideHCID 6228—
生成物5-(5-(Cyclopropylcarbamoyl)-2-methylphenylcarbamoyl)thiophen-2-ylboronic acidHCID 59761503178.3%

反応条件

温度90 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07935696B2
出典データセットuspto-grants-2011_05
ORD IDord-135ecc26917e4d76af946caa32bbb78a
出典メモuspto-grants-2011_05