Chemical Research in 21778-81-4

After consulting a lot of data, we found that this compound(21778-81-4)Safety of 5-Methoxy-1H-indole-2-carbaldehyde can be used in many types of reactions. And in most cases, this compound has more advantages.

The chemical properties of alicyclic heterocycles are similar to those of the corresponding chain compounds. Compound: 5-Methoxy-1H-indole-2-carbaldehyde, is researched, Molecular C10H9NO2, CAS is 21778-81-4, about Selective Synthesis of 5,6-Dihydroindolo-[1,2-a]quinoxalines and 6,7-Dihydroindolo-[2,3-c]quinolines by Orthogonal Copper and Palladium Catalysis, the main research direction is dihydroindoloquinoxaline dihydroindoloquinoline preparation copper palladium catalyst; Ugi four component reaction.Safety of 5-Methoxy-1H-indole-2-carbaldehyde.

In combination with the Ugi four-component reaction, two important indole-fused heterocycles were prepared in two steps from readily accessible starting materials. From the same set of Ugi adducts 5, 5,6-dihydroindolo[1,2-a]quinoxalines were rapidly generated in excellent yields by a copper-catalyzed N-H arylation pathway, whereas 6,7-dihydroindolo[2,3-c]quinolones were obtained by palladium-catalyzed C-H arylations in good yields without the protection of the indole N1 moiety. Microwave heating was used to accelerate these intramol. C-N and C-C bond-forming reactions performed under controlled reaction conditions.

After consulting a lot of data, we found that this compound(21778-81-4)Safety of 5-Methoxy-1H-indole-2-carbaldehyde can be used in many types of reactions. And in most cases, this compound has more advantages.

Reference:
Pyridazine – Wikipedia,
Pyridazine | C4H4N2 – PubChem