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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1655067생성일: 2026년 10월 27일

Nitrogen → 3-Fluoropyridine-2-sulfonamide

https://huagongshe.com/reaction/1655067

반응식

참여 물질

역할이름HCID투입량
반응물NitrogenHCID 947—
반응물Sodium ChlorideHCID 5234—
반응물Hydrofluoric AcidHCID 14917—
반응물Sodium BicarbonateHCID 516892—
반응물3-Aminopyridine-2-sulfonamideHCID 14943702—
반응물Sodium NitriteHCID 23668193—
용매Dimethyl SulfoxideHCID 679—
생성물3-Fluoropyridine-2-sulfonamideHCID 1995793070%

반응 단계

5.3 g (0.030 mol) of 3-aminopyridin-2-ylsulfonamide are dissolved in 12 ml of dimethyl sulfoxide, and the solution is added dropwise at 0° C. to 14.3 g (0.72 mol) of hydrogen fluoride (exothermal reaction). 2.4 g (0.035 mol) of sodium nitrite are then added in portions at 0° C. After one hour, the mixture is heated to 70° C. (evolution of N2). After the reaction mixture has cooled, it is added to an ice/water mixture, sodium bicarbonate and sodium chloride are added, and the mixture is then extracted with tetrahydrofuran and ethyl acetate. The combined extracts are washed with a saturated sodium chloride solution, dried with magnesium sulfate, filtered and evaporated. The residue is stirred in diethyl ether/petroleum ether. Filtration gives 3.7 g of 3-fluoropyridin-2-ylsulfonamide (Compound No. 3.001) of a melting point of +124° to +125° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05410063
출처 데이터셋uspto-grants-1995_04
ORD IDord-429577d82d2a4a40b7f728b09be5c3bf
출처 메모uspto-grants-1995_04