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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 335813생성일: 2026년 10월 24일

Chloroacetone → 1-(2'-amino-7-bromo-5'H-spiro[chromeno[2,3-b]pyridine-5,4'-oxazole]-3-yloxy)propan-2-one

https://huagongshe.com/ko/reaction/335813

반응식

참여 물질

역할이름HCID투입량
반응물ChloroacetoneHCID 6571—
반응물Potassium CarbonateHCID 11430—
반응물Sodium chloride dihydrateHCID 23713072—
반응물2'-amino-7-bromo-5'H-spiro[chromeno[2,3-b]pyridine-5,4'-oxazol]-3-olHCID 58466282—
용매DimethylformamideHCID 6228—
용매TetrahydrofuranHCID 8028—
생성물1-(2'-amino-7-bromo-5'H-spiro[chromeno[2,3-b]pyridine-5,4'-oxazole]-3-yloxy)propan-2-oneHCID 67383082—

반응 단계

A solution of 2′-amino-7-bromo-5′H-spiro[chromeno[2,3-b]pyridine-5,4′-oxazol]-3-ol (0.570 g, 1.637 mmol) in 5 mL DMF was treated with potassium carbonate (0.283 g, 2.047 mmol) and was allowed to stir at RT for 15 minutes. The reaction mixture was then cooled to 0° C. and 1-chloropropan-2-one (0.151 g, 1.637 mmol) was added as a solution in 1 mL THF. After stirring for one hour the reaction mixture was allowed to warm to RT and stir for 4 hours. The reaction mixture was poured into 1:1 water/brine, extracted with EtOAc (3×25 mL). The combined organics were dried over MgSO4 and concentrated. Purification of the crude residue by column chromatography provided 1-(2′-amino-7-bromo-5′H-spiro[chromeno[2,3-b]pyridine-5,4′-oxazole]-3-yloxy)propan-2-one. MS m/z=404.0 [M+H].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08883782B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-61ec904ad3f34565878323b55291e9a0
출처 메모uspto-grants-2014_11