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. Author manuscript; available in PMC: 2022 Jan 1.
Published in final edited form as: Synapse. 2020 Aug 6;75(1):e22183. doi: 10.1002/syn.22183

FIGURE 3.

FIGURE 3

Synthesis of IPPI and BrPPI. Azaindole 10 was reacted with 3-chloro-6-iodoisoquinoline 11 in dimethylformamide (DMF) in the presence of potassium tert-butoxide for 24 hr at 120°C to provide IPPI, 9. Similarly, azaindole 10 was reacted with 3-fluoro-6-bromoisoquinoline 12 in DMF in the presence of potassium tert-butoxide for 24 hr at 120°C to provide 6-bromo-3-(1H-pyrrolo[2,3-c] pyridine-1-yl)isoquinoline, BrPPI, 13