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HRID 2275998생성일: 2026년 10월 27일

Diisopropylamine → 2-Chloro-6-[[1-(hydroxymethyl)-2-methyl-propyl]amino]-4-(trifluoromethyl)pyridine-3-carbonitrile

https://huagongshe.com/reaction/2275998

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylamineHCID 7912—
반응물ChlorineHCID 24526—
반응물ValinolHCID 79019—
반응물2,6-Dichloro-4-(trifluoromethyl)nicotinonitrileHCID 2736726—
생성물2-Chloro-6-[[1-(hydroxymethyl)-2-methyl-propyl]amino]-4-(trifluoromethyl)pyridine-3-carbonitrileHCID 58265083—

반응 단계

Neat 3-cyano-2,6-dichloro-4-trifluoromethylpyridine (0.641 g, 6 mmol) (Compound 14) was added by pipette at a dropwise rate over 3 minutes to 2-amino-3-methyl-butan-1-ol (1.5 g, 6 mmol) (Compound 15). 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-[[1-(hydroxymethyl)-2-methyl-propyl]amino]-4-(trifluoromethyl)pyridine-3-carbonitrile (Compound 13) was isolated in 50% yield.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09131694B2
출처 데이터셋uspto-grants-2015_09
ORD IDord-2cefea86b50f4e97b24c53ebae68dd36
출처 메모uspto-grants-2015_09