Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 335992생성일: 2026년 10월 24일
Benzeneethanamine, alpha-methyl-, phosphate (1:1) → (S)-7-(2-fluoropyridin-3-yl)-3-(pyrimidin-2-yl)-5'H-spiro[chromeno[2,3-b]pyridine-5,4'-thiazol]-2'-amine
https://huagongshe.com/ko/reaction/335992
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Benzeneethanamine, alpha-methyl-, phosphate (1:1) | HCID 62885 | — |
| 반응물 | 2-(Tributylstannyl)pyrimidine | HCID 2763251 | — |
| 반응물 | (S)-3-bromo-7-(2-fluoropyridin-3-yl)-5'H-spiro[chromeno[2,3-b]pyridine-5,4'-thiazol]-2'-amine | HCID 67438436 | — |
| 용매 | 1,4-Dioxane | HCID 31275 | — |
| 생성물 | (S)-7-(2-fluoropyridin-3-yl)-3-(pyrimidin-2-yl)-5'H-spiro[chromeno[2,3-b]pyridine-5,4'-thiazol]-2'-amine | HCID 58466117 | 12% |
반응 단계
A vial was charged with (S)-3-bromo-7-(2-fluoropyridin-3-yl)-5′H-spiro[chromeno[2,3-b]pyridine-5,4′-thiazol]-2′-amine (100 mg, 0.23 mmol), AmPhos (15.97 mg, 0.023 mmol), 2-(tributylstannyl)pyrimidine (333 mg, 0.90 mmol) and dioxane (1.50 mL). The vial was purged with Ar (g), sealed, and heated to 100° C. overnight. After cooling to rt, crude was diluted with MeOH (3 mL) and purified with reverse phase HPLC. Fractions containing product were washed with saturated aq. NaHCO3 (15 mL) and extracted with ethyl acetate (1×100 mL). The combined organic layers were dried over sodium sulfate, filtered, and concentrated in vacuo to provide a white solid, (S)-7-(2-fluoropyridin-3-yl)-3-(pyrimidin-2-yl)-5′H-spiro[chromeno[2,3-b]pyridine-5,4′-thiazol]-2′-amine (12 mg, 0.027 mmol, 12% yield). MS m/z=443.0 [M+H]+. Calc'd for C23H15FN6OS: 442.47.
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-70fd3fccf6804686aae1e94a19690e67 |
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| 출처 메모 | uspto-grants-2014_11 |
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