Potassium Carbonate → 6-(2-Pyrrolidin-1-yl-ethoxy)-2-pyrrolo[1,2-c]pyrimidin-3-yl-chromen-4-one O-tert-butyl oxime

HRID 1853306Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1853306
[C:1]([O:5][N:6]=[C:7]1[C:16]2[C:11](=[CH:12][CH:13]=[C:14]([O:17][CH2:18][CH2:19]Cl)[CH:15]=2)[O:10][C:9]([C:21]2[N:26]=[CH:25][N:24]3[CH:27]=[CH:28][CH:29]=[C:23]3[CH:22]=2)=[CH:8]1)([CH3:4])([CH3:3])[CH3:2].C(=O)([O-])[O-].[K+].[K+].[NH:36]1[CH2:40][CH2:39][CH2:38][CH2:37]1>C(#N)C>[C:1]([O:5][N:6]=[C:7]1[C:16]2[C:11](=[CH:12][CH:13]=[C:14]([O:17][CH2:18][CH2:19][N:36]3[CH2:40][CH2:39][CH2:38][CH2:37]3)[CH:15]=2)[O:10][C:9]([C:21]2[N:26]=[CH:25][N:24]3[CH:27]=[CH:28][CH:29]=[C:23]3[CH:22]=2)=[CH:8]1)([CH3:4])([CH3:3])[CH3:2]

Komponenten

5

Versuchsvorschrift

A mixture of 6-(2-chloro-ethoxy)-2-pyrrolo[1,2-c]pyrimidin-3-yl-chromen-4-one O-tert-butyl oxime (example 87B) (64 mg, 0.16 mmol), potassium carbonate (64 mg, 0.46 mmol) and pyrrolidine (19 μl, 0.24 mmol), in acetonitrile (1.5 ml) was heated in a sealed tube at 100° C. for 18 hours. The yellow suspension was filtered, the solid washed with ethyl acetate and the combined filtrates concentrated to dryness. The residue was purified by silica gel flash chromatography (gradient ethyl acetate/methanol 0-2%) to yield the title compound (49 mg, 71%) as a yellow solid.

Aufarbeitung

  1. filtrationThe yellow suspension was filtered
  2. washthe solid washed with ethyl acetate
  3. concentrationthe combined filtrates concentrated to dryness
  4. customThe residue was purified by silica gel flash chromatography (gradient ethyl acetate/methanol 0-2%)

Quellen und Nachweise

ORD-Eintrag
ord-9cd89519f34c43918a49b565ebacd8a8
Quelldatensatz
uspto-grants-2015_02
Patentnummer
US08962627B2

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