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Pyridine → N-(6-methoxypyridin-3-yl)cyclopropanecarboxamide

HRID 330231
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HRID 330231 반응식
[NH2:1][C:2]1[CH:3]=[CH:4][C:5]([O:8][CH3:9])=[N:6][CH:7]=1.N1C=CC=CC=1.[CH:16]1([C:19](Cl)=[O:20])[CH2:18][CH2:17]1>ClCCl>[CH3:9][O:8][C:5]1[CH:4]=[CH:3][C:2]([NH:1][C:19]([CH:16]2[CH2:18][CH2:17]2)=[O:20])=[CH:7][N:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 1049PyridineHCID 77637Cyclopropanecarbonyl chlorideHCID 811216-Methoxy-3-pyridinylamine

생성물 1

HCID 86308N-(6-methoxypyridin-3-yl)cyclopropanecarboxamide

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

5-Amino-2-methoxy pyridine (12.4 grams, 0.10 mole) and 10 milliliters (ml) of pyridine were mixed together in 200 ml dichloromethane in a reaction flask. 9.1 ml (0.10 mole) of cyclopropane carboxylic acid chloride was added to the reaction mixture over a period of 2 minutes. The reaction was exothermic and temperature rose to 34° C. The reaction was allowed to stand for one hour at room temperature, after which the reaction mixture was washed with 200 ml of 5% sodium hydroxide and 100 ml of water. The resulting organic phase was separated and dried over anhydrous magnesium sulfate. Crystals formed, so the mixture was filtered and washed with 300 ml of acetone and the filtrate evaporated in vacuo to give a solid that was triturated with hexane to yield 16.7 grams, after drying. The product was identified by IR and NMR as the title compound, having a melting point of 130°-131° C. This compound will be referred to as Compound 1.

후처리

  1. customrose to 34° C
  2. washafter which the reaction mixture was washed with 200 ml of 5% sodium hydroxide and 100 ml of water
  3. customThe resulting organic phase was separated
  4. dry with materialdried over anhydrous magnesium sulfate
  5. customCrystals formed, so the mixture
  6. filtrationwas filtered
  7. washwashed with 300 ml of acetone
  8. customthe filtrate evaporated in vacuo
  9. customto give a solid
  10. customthat was triturated with hexane
  11. customto yield 16.7 grams
  12. customafter drying

출처 및 근거

ORD 기록
ord-b03daed8ef034dc58d30eb23531e1e09
출처 데이터셋
uspto-grants-1990_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04895858

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