1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → N-(4-tert-butyl-phenyl)-2,6-difluoro-nicotinamide

HRID 2212720Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2212720
[F:1][C:2]1[C:7]([C:8]([OH:10])=O)=[CH:6][CH:5]=[C:4]([F:11])[N:3]=1.F[C:13]1[C:18]([C:19](O)=O)=[CH:17]C=CN=1.C([NH:26][C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1)(C)(C)C.C1C=CC2N(O)N=NC=2C=1.CCN=C=NCCCN(C)C.CCN(C(C)C)C(C)C>C(Cl)Cl>[F:1][C:2]1[C:7]([C:8]([NH:26][C:27]2[CH:28]=[CH:29][C:30]([C:18]([CH3:19])([CH3:13])[CH3:17])=[CH:31][CH:32]=2)=[O:10])=[CH:6][CH:5]=[C:4]([F:11])[N:3]=1

Komponenten

8

Versuchsvorschrift

A solution of 2,6-difluoropyridine-3-carboxylic acid (prepared similar to that described for 2-fluoropyridine-3-carboxylic acid, Example 64) (3.2 g, 20 mmol), t-butylaniline 11 (3.0 g, 20 mmol), HOBt (2.6 g, 20 mmol), EDAC (8 g, 40 mmole), and DIEA (8 mL) in CH2Cl2 (80 mL) was stirred at RT for 1 h. The mixture was washed with aq. NaHCO3 and brine. The organic solution was dried over Na2SO4 and concentrated in vacuo. The residue was purified via flash chromatography on silica (Hex:EtOAc=4:1) to give a light yellow flaky crystal as the desired product.

Aufarbeitung

  1. washThe mixture was washed with aq. NaHCO3 and brine
  2. dry with materialThe organic solution was dried over Na2SO4
  3. concentrationconcentrated in vacuo
  4. customThe residue was purified via flash chromatography on silica (Hex:EtOAc=4:1)

Quellen und Nachweise

ORD-Eintrag
ord-5f92ff36deba46d19f0bfbe2eeba7ca8
Quelldatensatz
uspto-grants-2006_09
Patentnummer
US07102009B2

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