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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 18002생성일: 2026년 10월 24일

1-Bromo-2-Chloroethane → HCID 59344699, 화합물

https://huagongshe.com/ko/reaction/18002

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참여 물질

역할이름HCID투입량
반응물1-Bromo-2-ChloroethaneHCID 7849—
반응물Methanol, magnesium salt (2:1)HCID 164537—
반응물HCID 178484497HCID 178484497—
용매Hydrochloric AcidHCID 313—
용매Dimethyl SulfoxideHCID 679—
용매MethanolHCID 887—
용매Ethyl AcetateHCID 8857—
생성물HCID 59344699HCID 59344699—

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온도60 °C

반응 단계

A mixture of 6-(3-chloro-4-fluorobenzyl)-3,4-dihydroxy-N,N-dimethyl-5-oxo-5,6,7,8-tetrahydro-2,6-naphthyridine-1-carboxamide (0.15 g, 0.39 μmmol; Example 1, Step 9) and magnesium methoxide in methanol (2 mL, 6-10% methanol solution available from Aldrich) in DMSO (4 mL) was heated at 60° C. for 30 minutes. Methanol was exhaustively removed under vacuum over 45 minutes. The resultant DMSO solution was treated with 1-bromo-2-chloroethane (0.28 g, 1.97 mmol) and stirred at 60° C. under an atmosphere of nitrogen overnight. The reaction mixture was diluted with ethyl acetate and dilute hydrochloric acid. The organic extract was washed with aqueous sodium sulfite, brine, dried over anhydrous sodium sulfate, filtered, and concentrated under vacuum. The residue was purified by reverse phase high pressure liquid chromatography. Collection and lyophilization of appropriate fractions provided the title compound, which was recrystallized from a mixture of ethyl acetate and hexane

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07741315B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-bbf1e97e41e7415cb36be5abda3e68d2
출처 메모uspto-grants-2010_06