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HRID 2276000생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/2276000

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 번호US09131694B2
출처 데이터셋uspto-grants-2015_09
ORD IDord-6dfd08c581e74732b0ee67d9ccb2f6a6
출처 메모uspto-grants-2015_09