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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 513192생성일: 2026년 10월 25일

Cesium fluoride → methyl 4-(2-fluoropyridin-4-yl)-1H-pyrrolo[3,2-c]pyridine-2-carboxylate

https://huagongshe.com/reaction/513192

반응식

참여 물질

역할이름HCID투입량
반응물Cesium fluorideHCID 25953—
반응물2-Fluoro-4-(tributylstannyl)pyridineHCID 16427099—
반응물1-Tert-butyl 2-methyl 4-chloro-1H-pyrrolo[3,2-C]pyridine-1,2-dicarboxylateHCID 71743059—
촉매HCID 178418851HCID 178418851—
용매1,4-DioxaneHCID 31275—
생성물methyl 4-(2-fluoropyridin-4-yl)-1H-pyrrolo[3,2-c]pyridine-2-carboxylateHCID 7121287177%

반응 조건

온도100 °C

반응 단계

1-Tert-butyl 2-methyl 4-chloro-1H-pyrrolo[3,2-c]pyridine-1,2-dicarboxylate (100 mg, 0.322 mmole), 2-fluoro-4-(tributylstannyl)pyridine (162 mg, 0.418 mmole), CsF (108 mg, 0.708 mmole), and bis(tri-t-butylphosphine)palladium(0) (16 mg, 0.031 mmole) were combined in a screw cap vial. To this was added 1,4-dioxane (1 mL). N2 was bubbled through the mixture for 10 seconds. The vial was capped then heated to 100° C. After 6 hr was cooled to RT, diluted with EtOAc, filtered through a pad of Celite washing with EtOAc, and concentrated. The residue was taken up in 2 mL CH2Cl2. To this was added 2 mL TFA. After 2 hr the mixture was concentrated. The residue was taken up in saturated NaHCO3 and extracted with CH2Cl2 (3×). The combined organic layers were dried (MgSO4), filtered, and concentrated. Flash column chromatography (Biotage-SNAP-10 g SiO2, 70% EtOAc/hexanes) gave the title compound (67 mg, 77%) as an off-white solid. 1H NMR (400 MHz, CDCl3): δ 9.23 (bs, 1 H); 8.56 (d, J=5.8 Hz, 1 H); 8.40 (d, J=5.2 Hz, 1 H); 7.82-7.79 (m, 1 H); 7.56 (s, 1 H); 7.50 (dd, J=2.0, 1.1 Hz, 1 H); 7.43 (dd, J=5.8, 1.1 Hz, 1 H); 4.00 (s, 3 H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09102673B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-8cbfd12dd1c3428180e4299ead8cb923
출처 메모uspto-grants-2015_08