Triethylamine → 1-{[(3-Nitroquinolin-4-yl)amino]methyl}cyclobutanol

HRID 44706

反応式

HRID 44706 の反応式
[NH2:1][CH2:2][C:3]1([OH:7])[CH2:6][CH2:5][CH2:4]1.C(N(CC)CC)C.Cl[C:16]1[C:25]2[C:20](=[CH:21][CH:22]=[CH:23][CH:24]=2)[N:19]=[CH:18][C:17]=1[N+:26]([O-:28])=[O:27]>ClCCl>[N+:26]([C:17]1[CH:18]=[N:19][C:20]2[C:25]([C:16]=1[NH:1][CH2:2][C:3]1([OH:7])[CH2:6][CH2:5][CH2:4]1)=[CH:24][CH:23]=[CH:22][CH:21]=2)([O-:28])=[O:27]

参加物

5

実験手順

To a solution of 1-(aminomethyl)cyclobutanol (62.5 mmol) in dichloromethane (312 mL) was added triethylamine (8.71 mL, 62.5 mmol) and 4-chloro-3-nitroquinoline (13.04 g, 62.5 mmol). More triethylamine (3 mL) was added almost immediately. The reaction was stirred under N2 for 10 d at rt, then was diluted with dichloromethane and washed with 1 M aqueous NaOH. A solid formed and was isolated by filtration. The organic layer was washed with water and brine, dried over Na2SO4, filtered, and concentrated to a solid that was crystallized from isopropanol. The resulting crystals were combined with the solid that was isolated from the extraction and the mixture was triturated with hot isopropanol. The solid was isolated by filtration, washed with diethyl ether, and air dried to yield 1-{[(3-nitroquinolin-4-yl)amino]methyl}cyclobutanol as yellow crystals. (12.83 g, 75%).

後処理

  1. washwashed with 1 M aqueous NaOH
  2. customA solid formed
  3. customwas isolated by filtration
  4. washThe organic layer was washed with water and brine
  5. dry with materialdried over Na2SO4
  6. filtrationfiltered
  7. concentrationconcentrated to a solid
  8. customthat was crystallized from isopropanol
  9. customthat was isolated from the extraction
  10. customthe mixture was triturated with hot isopropanol
  11. customThe solid was isolated by filtration
  12. washwashed with diethyl ether, and air
  13. customdried

出典と根拠

ORDレコード
ord-220d0047b7ff4594bc9afa7e60146efa
出典データセット
uspto-grants-2013_09
特許番号
US08541438B2

関連ノート

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