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

HRID 35207

反応式

HRID 35207 の反応式
[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

参加物

5

実験手順

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 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.

後処理

  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 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

出典と根拠

ORDレコード
ord-b7994748802144c7af236fb5891588e3
出典データセット
uspto-grants-1988_08
特許番号
US04766135

関連ノート

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