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Diisopropylcarbodiimide → CID 11765197

HRID 2290044
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HRID 2290044 반응식
[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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

9

반응물 5

HCID 12734DiisopropylcarbodiimideHCID 24436Sodium SulfateHCID 1385867TriethylammoniumHCID 86755573Chloroform butanol methanolHCID 178522910HCID 178522910, 화합물

생성물 1

HCID 178484780CID 11765197

시약·촉매·용매 3

HCID 14284
4-(Dimethylamino)pyridine
촉매
HCID 6342Acetonitrile용매
HCID 21956068Chloroform tetrahydrofuran용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-8d632bc8a2ab47c8a40a79fd73c3f0ff
출처 데이터셋
uspto-grants-2000_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06093732

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