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Diisopropylcarbodiimide → CID 11765197

HRID 2290044
ノート
印刷プレビュー

反応式

HRID 2290044 の反応式
[Cl:1][C:2]1[CH:27]=[CH:26][C:5]([CH2:6][NH:7][C:8]([C:10]2[CH:11]=[N:12][C:13]3[C:18]([C:19]=2[OH:20])=[CH:17][C:16]([CH2:21][CH2:22][CH2:23][OH:24])=[CH:15][C:14]=3[F:25])=[O:9])=[CH:4][CH:3]=1.[CH2:28]([NH+:30]([CH2:33][CH3:34])[CH2:31][CH3:32])C.C(N=C=N[CH:41]([CH3:43])[CH3:42])(C)C.[S:44]([O-:48])([O-])(=[O:46])=[O:45].[Na+:49].[Na+].C(Cl)(Cl)Cl.[CH2:55]([OH:59])[CH2:56][CH2:57]C.C[OH:61]>CN(C1C=CN=CC=1)C.C(#N)C.C1COCC1.C(Cl)(Cl)Cl>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:6][NH:7][C:8]([C:10]2[CH:11]=[N:12][C:13]3[C:18]([C:19]=2[OH:20])=[CH:17][C:16]([CH2:21][CH2:22][CH2:23][O:24][C:55](=[O:59])[CH2:56][CH2:57][CH2:43][CH2:41][CH2:42][CH2:32][C:31]([N:30]([CH3:28])[CH2:33][CH2:34][S:44]([O-:48])(=[O:46])=[O:45])=[O:61])=[CH:15][C:14]=3[F:25])=[O:9])=[CH:26][CH:27]=1.[Na+:49]
参加物実験手順後処理出典と根拠反応ノート

参加物

9

反応物 5

HCID 12734DiisopropylcarbodiimideHCID 24436Sodium SulfateHCID 1385867TriethylammoniumHCID 86755573Chloroform butanol methanolHCID 178522910HCID 178522910、化合物

生成物 1

HCID 178484780CID 11765197

試薬・触媒・溶媒 3

HCID 14284
4-(Dimethylamino)pyridine
触媒
HCID 6342Acetonitrile溶媒
HCID 21956068Chloroform tetrahydrofuran溶媒

実験手順

To a stirred mixture of 78 mg of N-(4-chlorobenzyl)-8-fluoro-4-hydroxy-6-(3-hydroxypropyl)-3-quinolinecarboxamide from Example No. 110, 27 mg of DMAP, and 0.46 mL of a 0.65 M solution of suleptanic acid triethylammonium salt in acetonitrile, in 1 mL of 1:1 THF-chloroform, was added 38 μL of diisopropylcarbodiimide. The solution was stirred for 18 h, then concentrated under reduced pressure. Flash chromatography of the residue on silica using 5-15% methanol in dichloromethane provided a solid. This was dissolved in chloroform-butanol-methanol, and the solution stirred with saturated aqueous sodium sulfate. The organic phase was filtered through anhydrous sodium sulfate and concentrated under reduced pressure to afford 121 mg of the title compound as a white solid.

後処理

  1. concentrationconcentrated under reduced pressure
  2. customFlash chromatography of the residue on silica using 5-15% methanol in dichloromethane provided a solid
  3. filtrationThe organic phase was filtered through anhydrous sodium sulfate
  4. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-8d632bc8a2ab47c8a40a79fd73c3f0ff
出典データセット
uspto-grants-2000_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06093732

反応ノート

読み込み中…

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