Dicyclohexylcarbodiimide → N-(2,3'-bipyridin-6'-yl)-2-(6-chloro-5-methylpyridin-3-yl)acetamide

HRID 1036202Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1036202
[Cl:1][C:2]1[N:7]=[CH:6][C:5]([CH2:8][C:9]([OH:11])=O)=[CH:4][C:3]=1[CH3:12].[N:13]1[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=1[C:19]1[CH:20]=[N:21][C:22]([NH2:25])=[CH:23][CH:24]=1.C1(N=C=NC2CCCCC2)CCCCC1>CN(C)C1C=CN=CC=1.CN(C=O)C>[N:13]1[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=1[C:19]1[CH:20]=[N:21][C:22]([NH:25][C:9](=[O:11])[CH2:8][C:5]2[CH:6]=[N:7][C:2]([Cl:1])=[C:3]([CH3:12])[CH:4]=2)=[CH:23][CH:24]=1

Komponenten

6

Edukt 3

HCID 10868DicyclohexylcarbodiimideHCID 124522625-(Pyridin-2-yl)pyridin-2-amineHCID 552673572-(6-Chloro-5-methylpyridin-3-yl)acetic acid

Produkt 1

HCID 58447789N-(2,3'-bipyridin-6'-yl)-2-(6-chloro-5-methylpyridin-3-yl)acetamide

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 142844-(Dimethylamino)pyridineKatalysatorHCID 6228DimethylformamideLösungsmittel

Versuchsvorschrift

A mixture of 2-(6-chloro-5-methylpyridin-3-yl)acetic acid 74-4 (57 mg, 0.31 mmol), 2,3′-bipyridin-6′-amine 124-1 (51 mg, 0.30 mmol), 1,3-dicyclohexylcarbodiimide (75 mg, 0.36 mmol) and 4-(dimethylamino)pyridine (6 mg, 0.06 mmol) in DMF (1.2 mL) was stirred at room temperature for 10 hours. The reaction mixture was filtered through celite, washed and diluted with ethyl acetate (30 ml) and extracted with water 930 ml×2). The organic phase was dried over Na2SO4 and concentrated by evaporation. The residue was subjected to silica gel column chromatography with ethyl acetate as eluent to give N-(2,3′-bipyridin-6′-yl)-2-(6-chloro-5-methylpyridin-3-yl)acetamide 124-2 as white solid.

Aufarbeitung

  1. filtrationThe reaction mixture was filtered through celite
  2. washwashed
  3. additiondiluted with ethyl acetate (30 ml)
  4. extractionextracted with water 930 ml×2)
  5. dry with materialThe organic phase was dried over Na2SO4
  6. concentrationconcentrated by evaporation

Quellen und Nachweise

ORD-Eintrag
ord-853cadc055cd4731b0338c3eae9065a4
Quelldatensatz
uspto-grants-2013_10
Patentnummer
US08546396B2

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