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HRID 280058생성일: 2026년 10월 27일

Ammonia → furo(3,4-b)pyridin-5(7H)-one

https://huagongshe.com/reaction/280058

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물IndoleHCID 798—
반응물Acetic AnhydrideHCID 7918—
반응물Furo[3,4-b]pyridine-5,7-dioneHCID 69688—
반응물Calcium ChlorideHCID 5284359—
반응물Aluminum(III) ChlorideHCID 6451240—
촉매Cupric ChlorideHCID 24014—
촉매Cobalt(II) chlorideHCID 24288—
촉매Ferrous ChlorideHCID 24458—
촉매ZincchlorideHCID 3007855—
용매Acetic AcidHCID 176—
용매AcetonitrileHCID 6342—
생성물furo(3,4-b)pyridin-5(7H)-oneHCID 819439—

반응 단계

A particularly advantageous embodiment of the novel process comprises dissolving or suspending quinolinic anhydride in a saturated aliphatic C2 -C4 -monocarboxylic acid, in particular acetic acid, or also in acetonitrile, adding an indole compound of the formula (7a) and stirring the mixture at room temperature in the presence of an inorganic metal salt, in particular a metal halide, of a polyvalent metal or atomic weight 26 to 66, for example zinc chloride, calcium chloride, aluminium chloride, iron chloride, cobalt chloride or copper dichloride, preferably for 2 to 6 hours. The compound of the formula (5a) is then added and, after addition of acetic anhydride, the reaction mixture is heated at 30° to 60° C., preferably for 1 to 3 hours. The pH is then adjusted to 7.5 to 9 for example with an alkali metal hydroxide or aqueous ammonia. The precipitated 4-azaphthalide compound of the formula (1a) is isolated and, if necessary, recrystallised.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04587539
출처 데이터셋uspto-grants-1986_05
ORD IDord-d0e8178ae6be475bb5721a445bedd9ae
출처 메모uspto-grants-1986_05