3-(2-methoxyphenyl)propanenitrile

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

Procedure: The title compound was synthesized according to EXAMPLE 11 from 2-amino-3-methoxybenzaldehyde and 3-(2-methoxyphenyl)propionitrile.

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

Procedure: The title compound was synthesized according to EXAMPLE 11 from 2-amino-4-fluoro-5-morpholin-4-ylbenzaldehyde and 3-(2-methoxyphenyl)propionitrile.

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

Procedure: The title compound was synthesized according to EXAMPLE 11 from 2-amino-4-fluoro-5-morpholin-4-ylbenzaldehyde and 3-(2-methoxyphenyl)propionitrile.

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

Procedure: The title compound was synthesized according to EXAMPLE 11 from 2-amino-5-morpholin-4-ylbenzaldehyde and 3-(2-methoxyphenyl)propionitrile.

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

Procedure: The title compound was synthesized according to EXAMPLE 11 from 2-amino-5-(2-methoxy-ethoxy)benzaldehyde and 3-(2-methoxyphenyl)propionitrile.

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

Procedure: The title compound was synthesized according to EXAMPLE 11 from 2-amino-4,5-difluorobenzaldehyde and 3-(2-methoxyphenyl)propionitrile.

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

Procedure: The title compound was synthesized according to EXAMPLE 11 from 2-amino-4-fluorobenzaldehyde and 3-(2-methoxyphenyl)propionitrile.

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

Procedure: The title compound was synthesized according to EXAMPLE 11 from 2-amino-4,5-difluorobenzaldehyde and 3-(2-methoxyphenyl)propionitrile.

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

Procedure: The title compound was synthesized according to EXAMPLE 11 from 3-amino-2-pyridine carboxaldehyde trifluoroacetate (in turn synthesized from (2-formylpyridin-3-yl)carbamate tert-butyl ester by treatment with trifluoroacetic acid) and 3-(2-methoxyphenyl)propionitrile. One equivalent of potassium tert-butylate was additionally used.

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

Procedure: The title compound was synthesized according to EXAMPLE 11 from 3-amino-4-pyridine carboxaldehyde and 3-(2-methoxyphenyl)propionitrile.

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

Procedure: The title compound was synthesized according to EXAMPLE 11 from 4-aminonicotinaldehyde and 3-(2-methoxyphenyl)propionitrile.

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

Procedure: The title compound was synthesized according to EXAMPLE 11 from 2-amino-5-ethoxybenzaldehyde and 3-(2-methoxyphenyl)propionitrile.