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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Chloroacetone | HCID 6571 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | Sodium chloride dihydrate | HCID 23713072 | — |
| 반응물 | 2'-amino-7-bromo-5'H-spiro[chromeno[2,3-b]pyridine-5,4'-oxazol]-3-ol | HCID 58466282 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 1-(2'-amino-7-bromo-5'H-spiro[chromeno[2,3-b]pyridine-5,4'-oxazole]-3-yloxy)propan-2-one | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08883782B2 |
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| 출처 데이터셋 | uspto-grants-2014_11 |
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| ORD ID | ord-61ec904ad3f34565878323b55291e9a0 |
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| 출처 메모 | uspto-grants-2014_11 |
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