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Phosphorus oxychloride → 1-(3-Chloropyridin-2-yl)-1,2,3,6-tetrahydropyridine-4-carbonitrile

HRID 404567
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반응식

HRID 404567 반응식
P(Cl)(Cl)(Cl)=O.[Cl:6][C:7]1[C:8]([N:13]2[CH2:18][CH2:17][C:16](O)([C:19]#[N:20])[CH2:15][CH2:14]2)=[N:9][CH:10]=[CH:11][CH:12]=1>N1C=CC=CC=1>[Cl:6][C:7]1[C:8]([N:13]2[CH2:14][CH:15]=[C:16]([C:19]#[N:20])[CH2:17][CH2:18]2)=[N:9][CH:10]=[CH:11][CH:12]=1
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참가 물질

4

반응물 2

HCID 24813Phosphorus oxychlorideHCID 714170321-(3-Chloropyridin-2-yl)-4-hydroxypiperidine-4-carbonitrile2회

생성물 1

HCID 583194961-(3-Chloropyridin-2-yl)-1,2,3,6-tetrahydropyridine-4-carbonitrile

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

At 0° C., phosphoryl trichloride (10 g, 68 mmol) was slowly added into a solution of 1-(3-chloropyridin-2-yl)-4-hydroxypiperidine-4-carbonitrile (compound 22) (8 g, 33 mmol) in pyridine. After stirred at RT for 30 minutes, the reaction was washed by a HCl solution, and extracted by ethyl acetate. The organic layer was evaporated to give a crude product, which was purified using column chromatography to give the product.

후처리

  1. washthe reaction was washed by a HCl solution
  2. extractionextracted by ethyl acetate
  3. customThe organic layer was evaporated

출처 및 근거

ORD 기록
ord-0baa843af5a34f44b8d1d413461c08d2
출처 데이터셋
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08748610B2

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