3-(benzoylamino)-5,6,7,8-tetrahydro-2,5-dioxo-1(2H)-quinolineacetic acid

Base Information

Chemical Name:3-(benzoylamino)-5,6,7,8-tetrahydro-2,5-dioxo-1(2H)-quinolineacetic acid
CAS No.:161038-37-5
Molecular Formula:C₁₈H₁₆N₂O₅
Molecular Weight:340.335
Hs Code.:

Synonyms:3-(benzoylamino)-5,6,7,8-tetrahydro-2,5-dioxo-1(2H)-quinolineacetic acid

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Chemical Property of 3-(benzoylamino)-5,6,7,8-tetrahydro-2,5-dioxo-1(2H)-quinolineacetic acid

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Technology Process of 3-(benzoylamino)-5,6,7,8-tetrahydro-2,5-dioxo-1(2H)-quinolineacetic acid

There total 2 articles about 3-(benzoylamino)-5,6,7,8-tetrahydro-2,5-dioxo-1(2H)-quinolineacetic acid which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 77.0%

: 161038-40-0
N-<1-<(azidocarbonyl)methyl>-1,2,5,6,7,8-hexahydro-2,5-dioxo-3-quinolinyl>benzamide

: 161038-43-3
N-(1,2,5,6,7,8-hexahydro-2,5-dioxo-3-quinolinyl)benzamide

: 161038-37-5
3-(benzoylamino)-5,6,7,8-tetrahydro-2,5-dioxo-1(2H)-quinolineacetic acid

Guidance literature:: With potassium hydroxide; at 0 ℃; for 30h;
DOI:10.1002/jhet.5570310601

Reference yield:

: 92856-34-3
3-benzoylamino-5-oxo-5,6,7,8-tetrahydrocoumarin

: 56-40-6,18875-39-3,25718-94-9
glycine

: 161038-37-5
3-(benzoylamino)-5,6,7,8-tetrahydro-2,5-dioxo-1(2H)-quinolineacetic acid

Guidance literature:: With sodium methylate; In N,N-dimethyl-formamide; for 0.416667h; Heating;
DOI:10.1002/jhet.5570310601

Reference yield:

: 161038-37-5
3-(benzoylamino)-5,6,7,8-tetrahydro-2,5-dioxo-1(2H)-quinolineacetic acid

: 161038-39-7
N-<1-(carbazoylmethyl)-1,2,5,6,7,8-hexahydro-5-hydrazono-2-oxo-3-quinolinyl>benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: HCl / Ambient temperature

2: hydrazine hydrate / ethanol / 16 h / Heating

With hydrogenchloride; hydrazine hydrate; In ethanol;
DOI:10.1002/jhet.5570310601