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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 40723생성일: 2026년 10월 24일

Dimethylformamide → [4-(5-Fluoro-oxazolo[5,4-b]pyridin-2-yl)-phenyl]-dimethyl-amine

https://huagongshe.com/ko/reaction/40723

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참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Potassium CarbonateHCID 11430—
반응물4-(Dimethylamino)benzoic acidHCID 12092—
반응물2,6-Difluoropyridin-3-amineHCID 45080006—
용매PyridineHCID 1049—
용매DichloromethaneHCID 6344—
생성물[4-(5-Fluoro-oxazolo[5,4-b]pyridin-2-yl)-phenyl]-dimethyl-amineHCID 4455512044%

반응 조건

온도150 °C

반응 단계

To a solution of 4-dimethylamino-benzoic acid (635 mg, 3.84 mmol) in CH2Cl2 (38 mL) was added 1-chloro-N,N-2-trimethylpropenylamine (0.51 mL, 3.84 mmol). Following formation of the resulting acid chloride, the reaction mixture was concentrated affording a residue that was dissolved in pyridine (7.8 mL) before 2,6-difluoro-pyridin-3-ylamine (500 mg, 3.84) was added in one portion. After an additional 1 h, the reaction mixture was concentrated to dryness affording a residue to which was added DMF (5 mL) and K2CO3 (531 mg, 3.84 mmol). The resulting mixture was heated by microwave to 150° C. for 10 min, after which the resulting mixture was filtered, concentrated and purified by silica gel flash chromatography (0 to 100% EtOAc in hexanes) to afford [4-(5-fluoro-oxazolo[5,4-b]pyridin-2-yl)-phenyl]-dimethyl-amine (430 mg, 1.67 mmol, 44%). ES MS (M+H+)=258; 1H NMR δ (ppm)(DMSO-d6): 8.28 (1H, dd, J=8.36, 7.14 Hz), 8.01-7.94 (2H, m), 7.24-7.18 (1H, m), 6.87 (2H, d, J=8.89 Hz), 3.05 (6H, s); HRMS m/z 258.1039 (C14H12FN3O+H+ requires 258.1037).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08530483B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-fbb6c45f2ab04212add4973a72946f87
출처 메모uspto-grants-2013_09