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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 579448생성일: 2026년 10월 24일

3-Bromo-7-hydroxy-4-methylchromen-2-one → 4-(7-Hydroxy-4-methyl-2-oxo-2H-chromen-3-yl)-N-(2-morpholinoethyl)benzamide

https://huagongshe.com/ko/reaction/579448

반응식

참여 물질

역할이름HCID투입량
반응물3-Bromo-7-hydroxy-4-methylchromen-2-oneHCID 5337545—
반응물(4-((2-Morpholinoethyl)carbamoyl)phenyl)boronic acidHCID 44119153—
촉매palladium(II) acetateHCID 167845—
촉매2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
용매WaterHCID 962—
용매1-EthoxyethanolHCID 10129898—
생성물4-(7-Hydroxy-4-methyl-2-oxo-2H-chromen-3-yl)-N-(2-morpholinoethyl)benzamideHCID 86683427182.2%

반응 조건

온도150 °C

반응 단계

A mixture of 3-bromo-7-hydroxy-4-methyl-2H-chromen-2-one (1) (7.66 g, 30 mmol), 4-(2-morpholmoethylcarbamoyl)phenylboronic acid (2) (10.02 g, 36 mmol), Na3PO4 (17.21 g, 105 mmol) in a mixture of ethoxyethanol (0.140 g) and water (14 g) was purged with Argon for five minutes in a 250 mL pressure vessel. Ligand Sphos (738 mg, 1.8 mmol) and Pd(OAc)2 (206 mg, 0.90 mmol) were added under an Argon atmosphere then the vessel was sealed and heated for 60 min in a 150° C. oil bath with strong stirring. This process was repeated once. Upon cooling, the reaction mixtures were filtered through a silica plug using CH2Cl2 and MeOH wash. The unified solutions were evaporated to 100 mL slowly diluted with water (100 mL) and crystallized at 0° C. The product was filtered, washed with 50% MeOH (2×50 mL) and dried to afford 22.33 g (9.1%) of the title compound. MS (ESI): 409 (M+H)+. 1H NMR (δ, DMSO (2.5 ppm)): 10.57 (s, br, 1H), 8.46 (t, 1H), 7.88 (d, 2H), 7.69 (d, 1H), 7.39 (d, 2H), 6.84 (dd, 1H), 6.76 (d, 1H), 3.57 (m, 4H), 3.40 and 2.48 (2q, 2×2H), 2.43 (m, 4H), 2.22 (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09040714B2
출처 데이터셋uspto-grants-2015_05
ORD IDord-4b4e25e9d8cc41d59f2eb2f28d04339b
출처 메모uspto-grants-2015_05