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Methanol → 1-(3-chloropyridin-2-yl)-1,2,3,6-tetrahydropyridine-4-carboxylic Acid

HRID 404568
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반응식

HRID 404568 반응식
[Cl:1][C:2]1[C:3]([N:8]2[CH2:13][CH:12]=[C:11]([C:14]#N)[CH2:10][CH2:9]2)=[N:4][CH:5]=[CH:6][CH:7]=1.[OH-:16].[Na+].C[OH:19]>C[Si](C)(C)C1C=C(C=CC=1)N>[Cl:1][C:2]1[C:3]([N:8]2[CH2:13][CH:12]=[C:11]([C:14]([OH:19])=[O:16])[CH2:10][CH2:9]2)=[N:4][CH:5]=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 887MethanolHCID 14798Sodium HydroxideHCID 583194961-(3-Chloropyridin-2-yl)-1,2,3,6-tetrahydropyridine-4-carbonitrile2회

생성물 1

HCID 219047271-(3-chloropyridin-2-yl)-1,2,3,6-tetrahydropyridine-4-carboxylic Acid

시약·촉매·용매 1

HCID 124888833-(Trimethylsilyl)aniline용매

실험 절차

A solution of 1-(3-chloropyridin-2-yl)-1,2,3,6-tetrahydropyridine-4-carbonitrile (compound 23) in 1 20 ml of NaOH (5 g, 125 mmol) water solution and methanol (20 ml) (V/V=1:1) was heated to reflux, and stirred overnight. The reaction was washed by a HCl solution in an ice bath, 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. temperatureto reflux
  2. washThe reaction was washed by a HCl solution in an ice bath
  3. extractionextracted by ethyl acetate
  4. customThe organic layer was evaporated

출처 및 근거

ORD 기록
ord-3ae6ca62ab2741cca19f859dc1aa984f
출처 데이터셋
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08748610B2

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