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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 331183생성일: 2026년 10월 25일

5-Aminopyridine-2-carbonitrile → 6-Cyanopyridine-3-sulfonyl chloride

https://huagongshe.com/reaction/331183

반응식

참여 물질

역할이름HCID투입량
반응물5-Aminopyridine-2-carbonitrileHCID 3871395—
반응물Sodium NitriteHCID 23668193—
반응물Thionylchloride waterHCID 86607486—
용매Hydrochloric AcidHCID 313—
용매WaterHCID 962—
생성물6-Cyanopyridine-3-sulfonyl chlorideHCID 4700319073.5%

반응 조건

온도-5 °C

반응 단계

In parallel, 5-amino-2-cyano pyridine (10 g, 0.084 mol) is dissolved in concentrated HCl (98 ml) and the mixture is cooled to −5° C. To this mixture is added dropwise over a period of 1 h a solution of NaNO2 (8.2 g, 0.118 mol) in water (50 ml), maintaining the reaction temperature between −5° C. and 0° C. This slurry is then added dropwise over a period of 1 h to the above reaction mixture (thionylchloride/water mixture), maintaining the reaction temperature between −5° C. and 0° C. (Note: The diazotized mixture should be also kept at −5° C. throughout the addition). As the addition proceeds, a white solid precipitates. When the addition is over, the reaction mixture is stirred for an additional hour. The precipitate is collected by filtration, washed with cold water and dried under vacuum to afford the title compound as light yellow solid (12.5 g, Yield 73.5%). 1H NMR (DMSO-d6:400 MHz) δ 14.49 (1H, s), 8.87 (1H, s), 8.11-8.14(1H, d), 8.0-8.03 (1H, d); HPLC (max plot) 97% Rt 1.155 min; LC/MS: m/z, M+, 202.8.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08877757B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-61891c2d11db4648bce15139c7c65684
출처 메모uspto-grants-2014_11