Acetic Acid → Tert-butyl [4-(3-hydroxy-3,8-dihydroimidazo[4,5-d]dipyrido[2,3-b:4',3'-f]azepin-2-yl)pyridin-3-yl]carbamate

HRID 1043484Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1043484
[N:1]1[C:6]2[NH:7][C:8]3[CH:18]=[N:17][CH:16]=[CH:15][C:9]=3/[C:10](=[N:13]/[OH:14])/[C:11](=O)[C:5]=2[CH:4]=[CH:3][CH:2]=1.[C:19]([O:23][C:24](=[O:34])[NH:25][C:26]1[CH:27]=[N:28][CH:29]=[CH:30][C:31]=1[CH:32]=O)([CH3:22])([CH3:21])[CH3:20].C([O-])(=O)C.[NH4+:39].C(O)(=O)C>C(OCC)(=O)C.O>[OH:14][N:13]1[C:10]2[C:9]3[CH:15]=[CH:16][N:17]=[CH:18][C:8]=3[NH:7][C:6]3[N:1]=[CH:2][CH:3]=[CH:4][C:5]=3[C:11]=2[N:39]=[C:32]1[C:31]1[CH:30]=[CH:29][N:28]=[CH:27][C:26]=1[NH:25][C:24](=[O:34])[O:23][C:19]([CH3:22])([CH3:21])[CH3:20]

Komponenten

7

Reaktionsbedingungen

Temperatur
80 °C

Versuchsvorschrift

A mixture of (6Z)-5H-dipyrido[2,3-b:4′,3′-f]azepine-5,6(11H)-dione 6-oxime (80.0 mg, 0.333 mmol), tert-butyl-(4-formylpyridin-3-yl)carbamate, ammonium acetate (0.513 g, 6.66 mmol), water (0.12 mL) and acetic acid (0.76 mL) was stirred at 80° C. for 3 h. The solution was diluted with ethyl acetate and water, the organic solution was washed with brine, dried over MgSO4 and concentrated. The crude residue was purified by preparative LCMS to yield the desired product (102 mg, 69%). LCMS for C23H22N2O3(M+H)+: m/z=444.2.

Aufarbeitung

  1. washthe organic solution was washed with brine
  2. dry with materialdried over MgSO4
  3. concentrationconcentrated
  4. customThe crude residue was purified by preparative LCMS

Quellen und Nachweise

ORD-Eintrag
ord-166f182f99d2494ca2d4e28802eaaf36
Quelldatensatz
uspto-grants-2013_10
Patentnummer
US08563541B2

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