[C:1]([C:5]1[C:12]([CH3:13])=[CH:11][C:8]([C:9]#[N:10])=[C:7](Cl)[N:6]=1)([CH3:4])([CH3:3])[CH3:2].ClC1C(C#N)=C[CH:19]=[C:18]([C:24]([CH3:27])([CH3:26])[CH3:25])N=1>>[C:1]([C:5]1[C:12]([CH3:13])=[CH:11][C:8]([C:9]#[N:10])=[C:7]([C:19]#[C:18][C:24]([CH3:27])([CH3:26])[CH3:25])[N:6]=1)([CH3:4])([CH3:3])[CH3:2]Procedure analogous to 31, using 62.6 g (300 mmol) of 6-tert-butyl-2-chloro-5-methylnicotinonitrile, S79, instead of 194.7 g (1 mol) of 2-chloro-3-cyano-6-tert-butylpyridine, S28, and scaling the remaining reagents correspondingly on a molar level. Yield: 68.9 g (271 mmol), 90%. Purity: >95% according to 1H-NMR.
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