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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1911819생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1911819

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 번호US08604199B2
출처 데이터셋uspto-grants-2013_12
ORD IDord-aeb529a6033640ed874ea6b5c4412dad
출처 메모uspto-grants-2013_12