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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1911821생성일: 2026년 10월 24일

Diisopropylamine → 2-Chloro-6-(2-hydroxybutylamino)-4-(trifluoromethyl)pyridine-3-carbonitrile

https://huagongshe.com/ko/reaction/1911821

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylamineHCID 7912—
반응물2-Amino-1-butanolHCID 22129—
반응물ChlorineHCID 24526—
반응물2,6-Dichloro-4-(trifluoromethyl)nicotinonitrileHCID 2736726—
생성물2-Chloro-6-(2-hydroxybutylamino)-4-(trifluoromethyl)pyridine-3-carbonitrileHCID 8665342155%

반응 단계

Neat 3-cyano-2,6-dichloro-4-trifluoromethylpyridine (0.641 g, 6 mmol) was added by pipette at a dropwise rate over 3 minutes to 2-aminobutanol (1.5 g, 6 mmol). Di-isopropylamine (0.9 g, 7 mmol) was added after 10 minutes and the resultant mixture was heated in a sealed tube at 70° C. for 30 minutes to selectively displace the chlorine at position 6 before quenching in ice-cold water and extracted with dichloromethane. Organic extracts were washed twice with water, dried over sodium sulfate and concentrated under reduced pressure. The residue was washed with diethylether and the resultant solid was used in the next step without further purification. 2-Chloro-6-(2-hydroxybutylamino)-4-(trifluoromethyl) pyridine-3-carbonitrile was isolated in 55% yield.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08604199B2
출처 데이터셋uspto-grants-2013_12
ORD IDord-fad227854cef4529aa8948823934ee13
출처 메모uspto-grants-2013_12