3-(azetidin-1-yl)-3-oxopropanenitrile

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: To a 50 ml three necked round bottom flask 4-(7-pivaloyl-5-((2-(trimethylsilyl)-ethoxy)methyl)-5H-pyrrolo[2,3-b]pyrazin-2-ylamino)benzaldehyde (0.13 g, 0.00029 mole) and 3-(azetidin-1-yl)-3-oxopropanenitrile (0.107 g, 0.00086 mole) was taken in ethanol (20 ml). To this reaction mixture, piperidine acetate (0.05 ml) was added drop wise at RT. After completion of the addition, the reaction mixture was refluxed for 2 hr. After completion of the reaction, ethanol was distilled out under vacuum and water was added to the residue. The aq. layer was extracted with ethyl acetate and the combined organic layer was dried over Na2SO4, filtered and concentrated to afford crude product. The crude compound was purified by triturated with n-pentane, pentane layer was decanted and solid was dried under vacuum to yield 0.14 g of 2-(azetidine-1-carbonyl)-3-(4-(7-pivaloyl-5-((2-(trimethylsilyl)ethoxy)-methyl)-5H-pyrrolo[2,3-b]pyrazin-2-ylamino)phenyl)acrylonitrile which was converted to the title compound as described in Example 1, Step 2. After completion of the addition the reaction mixture was refluxed for 2 hr was distilled out under vacuum and water was added to the residue The aq. layer was extracted with ethyl acetate the combined organic layer was dried over Na2SO4 filtered concentrated to afford crude product The crude compound was purified by triturated with n-pentane, pentane layer was decanted solid was dried under vacuum

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: To a 50 ml three necked round bottom flask 4-(7-pivaloyl-5-((2-(trimethylsilyl)-ethoxy)methyl)-5H-pyrrolo[2,3-b]pyrazin-2-ylamino)benzaldehyde (0.13 g, 0.00029 mole) and 3-(azetidin-1-yl)-3-oxopropanenitrile (0.107 g, 0.00086 mole) was taken in ethanol (20 ml). To this reaction mixture, piperidine acetate (0.05 ml) was added drop wise at RT. After completion of the addition, the reaction mixture was refluxed for 2 hr. After completion of the reaction, ethanol was distilled out under vacuum and water was added to the residue. The aq. layer was extracted with ethyl acetate and the combined organic layer was dried over Na2SO4, filtered and concentrated to afford crude product. The crude compound was purified by triturated with n-pentane, pentane layer was decanted and solid was dried under vacuum to yield 0.14 g of 2-(azetidine-1-carbonyl)-3-(4-(7-pivaloyl-5-((2-(trimethylsilyl)ethoxy)-methyl)-5H-pyrrolo[2,3-b]pyrazin-2-ylamino)phenyl)acrylonitrile which was converted to the title compound as described in Example 1, Step 2. After completion of the addition the reaction mixture was refluxed for 2 hr was distilled out under vacuum and water was added to the residue The aq. layer was extracted with ethyl acetate the combined organic layer was dried over Na2SO4 filtered concentrated to afford crude product The crude compound was purified by triturated with n-pentane, pentane layer was decanted solid was dried under vacuum

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: To a 50 ml three necked round bottom flask 4-(7-pivaloyl-5-((2-(trimethylsilyl)-ethoxy)methyl)-5H-pyrrolo[2,3-b]pyrazin-2-ylamino)benzaldehyde (0.13 g, 0.00029 mole) and 3-(azetidin-1-yl)-3-oxopropanenitrile (0.107 g, 0.00086 mole) was taken in ethanol (20 ml). To this reaction mixture, piperidine acetate (0.05 ml) was added drop wise at RT. After completion of the addition, the reaction mixture was refluxed for 2 hr. After completion of the reaction, ethanol was distilled out under vacuum and water was added to the residue. The aq. layer was extracted with ethyl acetate and the combined organic layer was dried over Na2SO4, filtered and concentrated to afford crude product. The crude compound was purified by triturated with n-pentane, pentane layer was decanted and solid was dried under vacuum to yield 0.14 g of 2-(azetidine-1-carbonyl)-3-(4-(7-pivaloyl-5-((2-(trimethylsilyl)ethoxy)-methyl)-5H-pyrrolo[2,3-b]pyrazin-2-ylamino)phenyl)acrylonitrile which was converted to the title compound as described in Example 1, Step 2. After completion of the addition the reaction mixture was refluxed for 2 hr was distilled out under vacuum and water was added to the residue The aq. layer was extracted with ethyl acetate the combined organic layer was dried over Na2SO4 filtered concentrated to afford crude product The crude compound was purified by triturated with n-pentane, pentane layer was decanted solid was dried under vacuum