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- W2950795409 abstract "A four-step synthesis of 5-carboxamidopyrrolo[3,2-b]pyridine (3) from pyrrolo[3,2-b]pyridine (4) is described (45% overall yield). The one-step conversion of the N-oxide 6 of the pyrrolo[3,2-b]pyridine 5 leads to the 5-cyanopyrrolo[3,2-b]pyridine 7. The cyano group is hydrolyzed to afford the title compound 3, which is the 4-aza analog of the indole backbone in 5-carboxamidotryptamine, a potent agonist of the neurotransmitter, serotonin." @default.
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- W2950795409 date "1992-10-01" @default.
- W2950795409 modified "2023-09-23" @default.
- W2950795409 title "A synthesis of 5-carboxamidopyrrolo[3,2-b]pyridine" @default.
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- W2950795409 doi "https://doi.org/10.1002/jhet.5570290616" @default.
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