Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diisopropylamine | HCID 7912 | — |
| 반응물 | Chlorine | HCID 24526 | — |
| 반응물 | Valinol | HCID 79019 | — |
| 반응물 | 2,6-Dichloro-4-(trifluoromethyl)nicotinonitrile | HCID 2736726 | — |
| 생성물 | 2-Chloro-6-[[1-(hydroxymethyl)-2-methyl-propyl]amino]-4-(trifluoromethyl)pyridine-3-carbonitrile | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09131694B2 |
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| 출처 데이터셋 | uspto-grants-2015_09 |
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| ORD ID | ord-2cefea86b50f4e97b24c53ebae68dd36 |
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| 출처 메모 | uspto-grants-2015_09 |
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