N-Methylpiperidine → N1-[1-(5-chloro-6-ethyl-4-pyrimidinyloxy)-2-propyl]-N2-isopropoxycarbonyl-L-valinamide

HRID 1900200ノート

反応式

HRID 1900200 の反応式
CN1CCCCC1.[CH:8]([O:11][C:12]([NH:14][C@H:15]([C:19]([OH:21])=O)[CH:16]([CH3:18])[CH3:17])=[O:13])([CH3:10])[CH3:9].ClC(OCC(C)C)=O.[Cl:30][C:31]1[C:32]([O:39][CH2:40][CH:41]([NH2:43])[CH3:42])=[N:33][CH:34]=[N:35][C:36]=1[CH2:37][CH3:38]>C(Cl)Cl.O>[Cl:30][C:31]1[C:32]([O:39][CH2:40][CH:41]([NH:43][C:19](=[O:21])[C@H:15]([CH:16]([CH3:17])[CH3:18])[NH:14][C:12]([O:11][CH:8]([CH3:9])[CH3:10])=[O:13])[CH3:42])=[N:33][CH:34]=[N:35][C:36]=1[CH2:37][CH3:38]

参加物

7

反応物 4

HCID 12291N-MethylpiperidineHCID 62365Isobutyl chloroformateHCID 11063514(2S)-3-methyl-2-(((propan-2-yloxy)carbonyl)amino)butanoic acidHCID 537174511-(5-Chloro-6-ethyl-4-pyrimidinyloxy)-2-propylamine

生成物 1

HCID 54207334N1-[1-(5-chloro-6-ethyl-4-pyrimidinyloxy)-2-propyl]-N2-isopropoxycarbonyl-L-valinamide収率 43.6%

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 6344Dichloromethane溶媒

反応条件

温度
-20 °C

実験手順

0.34 g of N-methylpiperidine was added to a solution containing 0.7 g of N-isopropoxycarbonyl-L-valine dissolved in 50 ml of methylene chloride, at -20° C. After the mixture was stirred for 10 minutes at the same temperature, 0.47 g of isobutyl chloroformate was added to the mixture, and stirred for 1 hour at -20° C. 0.74 g of 1-(5-chloro-6-ethyl-4-pyrimidinyloxy)-2-propylamine was added to this mixture at -60° C., and then the reaction mixture was allowed to sit and warm naturally to room temperature while being stirred, and was stirred for 20 hours at room temperature. Water was subsequently added to the reaction mixture. After the methylene chloride layer was washed successively with a 5% aqueous solution of sodium bicarbonate and water, the organic layer was dried over anhydrous magnesium sulfate and the methylene chloride was removed under reduced pressure. The obtained crude crystal was purified by column chromatography on silica gel, thus obtaining 0.6 g of the desired product in the form of a white prism-shaped crystal (yield: 43%).

後処理

  1. additionwas added to the mixture
  2. temperaturewarm naturally to room temperature
  3. stirringwhile being stirred
  4. stirringwas stirred for 20 hours at room temperature
  5. washAfter the methylene chloride layer was washed successively with a 5% aqueous solution of sodium bicarbonate and water
  6. dry with materialthe organic layer was dried over anhydrous magnesium sulfate
  7. customthe methylene chloride was removed under reduced pressure
  8. customThe obtained crude crystal
  9. customwas purified by column chromatography on silica gel

出典と根拠

ORDレコード
ord-65c4eea05fee4d29a45b2df41fc06177
出典データセット
uspto-grants-1996_11
特許番号
US05574064

反応ノート

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