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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 575119생성일: 2026년 10월 24일

9-Bromo-4-oxo-4,5-dihydro-6-oxa-3-thia-1-aza-benzo[e]azulene-2-carboxylic acid methyl ester → 9-Bromo-4-hydroxy-4-methyl-4,5-dihydro-6-oxa-3-thia-1-aza-benzo[e]azulene-2-carboxylic acid methyl ester

https://huagongshe.com/ko/reaction/575119

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참여 물질

역할이름HCID투입량
반응물9-Bromo-4-oxo-4,5-dihydro-6-oxa-3-thia-1-aza-benzo[e]azulene-2-carboxylic acid methyl esterHCID 86693085—
반응물HCID 178418689HCID 178418689—
용매TetrahydrofuranHCID 8028—
생성물9-Bromo-4-hydroxy-4-methyl-4,5-dihydro-6-oxa-3-thia-1-aza-benzo[e]azulene-2-carboxylic acid methyl esterHCID 8669314674.1%

반응 조건

온도-70 °C

반응 단계

To a stirred solution of 9-Bromo-4-oxo-4,5-dihydro-6-oxa-3-thia-1-aza-benzo[e]azulene-2-carboxylic acid methyl ester (500 mg, 1.41 mmol) in THF (20 mL) at −70° C., was added MeMgBr (1.8 M in THF, 1.57 mL, 2.82 mmol) dropwise. The reaction was stirred at −70° C. for 3 h, and then warmed to −30° C. for 1 h. The reaction mixture was quenched with saturated aqueous NH4Cl solution at −30° C. and extracted with EtOAc (20 mL×2). The combined organic layers were washed with brine, dried over Na2SO4, concentrated and purified by flash column chromatography (silica gel, EtOAc in hexane from 0 to 30%) to give 9-Bromo-4-hydroxy-4-methyl-4,5-dihydro-6-oxa-3-thia-1-aza-benzo[e]azulene-2-carboxylic acid methyl ester as a yellow solid (387 mg, 74%) LC-MS (ESI & APCI): 372.2 (M+2).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09034866B2
출처 데이터셋uspto-grants-2015_05
ORD IDord-f6db10218ef741e2a8e22080bade7aa5
출처 메모uspto-grants-2015_05