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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 407258생성일: 2026년 10월 24일

Acetonitrile → HCID 71150699, 화합물

https://huagongshe.com/ko/reaction/407258

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참여 물질

역할이름HCID투입량
반응물AcetonitrileHCID 6342—
반응물Cesium fluorideHCID 25953—
반응물(6-Methoxypyridin-3-yl)boronic acidHCID 2734368—
반응물Methyl 4-amino-6-chloro-5-fluoro-3-methoxypicolinateHCID 86675409—
촉매Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
용매WaterHCID 962—
용매1,4-DioxaneHCID 31275—
용매Sodium chloride; waterHCID 57417360—
생성물HCID 71150699HCID 7115069928.4%

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온도85 °C

반응 단계

To a tube, methyl 4-amino-6-chloro-5-fluoro-3-methoxypicolinate (500 mg, 2.131 mmol), (6-methoxypyridin-3-yl)boronic acid (391 mg, 2.56 mmol), [1,1′-Bis(diphenylphosphino)ferrocene]dichloropalladium(II) (78 mg, 0.107 mmol) and Cesium Fluoride (647 mg, 4.26 mmol) were charged as solids. The tube was sealed and charged with inert atmosphere. The solids were then diluted with Dioxane (5700 μl) and Water (1400 μl). The resulting suspension was heated to 85° C. for 18 hrs. The reaction solution was poured in to a brine solution. The aqueous phase was extracted with EtOAc (3×25 mL). The combined organic layers were dried over MgSO4, filtered and concentrated under vacuum. The product was purified (flash chromatography: silica, 5-50% EtOAc in Hex 16 CV; C18 5-100% ACN in H2O 16 CV) to yield methyl 4-amino-3-fluoro-5,6′-dimethoxy-[2,3′-bipyridine]-6-carboxylate (186 mg, 0.605 mmol, 28.4% yield). ESIMS for m/z 308 (M+H)+. 1H NMR (400 MHz, DMSO-d6) δ 3.77 (s, 3H), 3.86 (s, 3H), 3.92 (s, 3H), 6.53 (s, 2H), 6.95 (dd, J=8.6, 0.8 Hz, 1H), 8.10 (ddd, J=8.6, 2.4, 1.1 Hz, 1H), 8.58 (t, J=2.0 Hz, 1H). 19F NMR (376 MHz, DMSO-d6) δ −141.20.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08754229B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-133516b77e0e46818f6bc5a227386ebe
출처 메모uspto-grants-2014_06