4-[2-(4-Amino-phenyl)-2-oxo-ethyl]-2-imino-5-methoxy-8-methyl-6-oxo-3,4-dihydro-2H,6H-pyrano[3,2-g]chromene-3-carboxylic acid amide

Base Information

Chemical Name:4-[2-(4-Amino-phenyl)-2-oxo-ethyl]-2-imino-5-methoxy-8-methyl-6-oxo-3,4-dihydro-2H,6H-pyrano[3,2-g]chromene-3-carboxylic acid amide
CAS No.:174088-07-4
Molecular Formula:C₂₃H₂₁N₃O₆
Molecular Weight:435.436
Hs Code.:

Synonyms:4-[2-(4-Amino-phenyl)-2-oxo-ethyl]-2-imino-5-methoxy-8-methyl-6-oxo-3,4-dihydro-2H,6H-pyrano[3,2-g]chromene-3-carboxylic acid amide

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Chemical Property of 4-[2-(4-Amino-phenyl)-2-oxo-ethyl]-2-imino-5-methoxy-8-methyl-6-oxo-3,4-dihydro-2H,6H-pyrano[3,2-g]chromene-3-carboxylic acid amide

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Technology Process of 4-[2-(4-Amino-phenyl)-2-oxo-ethyl]-2-imino-5-methoxy-8-methyl-6-oxo-3,4-dihydro-2H,6H-pyrano[3,2-g]chromene-3-carboxylic acid amide

There total 3 articles about 4-[2-(4-Amino-phenyl)-2-oxo-ethyl]-2-imino-5-methoxy-8-methyl-6-oxo-3,4-dihydro-2H,6H-pyrano[3,2-g]chromene-3-carboxylic acid amide 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: 56.4%

: 174088-01-8
6-[(E)-3-(4-Amino-phenyl)-3-oxo-propenyl]-7-hydroxy-5-methoxy-2-methyl-chromen-4-one

: 107-91-5
cyanoacetic acid amide

: 174088-07-4
4-[2-(4-Amino-phenyl)-2-oxo-ethyl]-2-imino-5-methoxy-8-methyl-6-oxo-3,4-dihydro-2H,6H-pyrano[3,2-g]chromene-3-carboxylic acid amide

Guidance literature:: With piperidine; In ethanol; for 30h; Heating;

Reference yield:

: 7338-51-4
7-hydroxy-5-methoxy-2-methyl-4-oxo-4H-chromene-6-carbaldehyde

: 174088-07-4
4-[2-(4-Amino-phenyl)-2-oxo-ethyl]-2-imino-5-methoxy-8-methyl-6-oxo-3,4-dihydro-2H,6H-pyrano[3,2-g]chromene-3-carboxylic acid amide

Guidance literature:: Multi-step reaction with 2 steps

1: 116 percent / 10percent NaOH / ethanol / 12 h / Ambient temperature

2: 56.4 percent / piperidine / ethanol / 30 h / Heating

With piperidine; sodium hydroxide; In ethanol;

Reference yield:

: 99-92-3
p-aminobenzophenone

: 174088-07-4
4-[2-(4-Amino-phenyl)-2-oxo-ethyl]-2-imino-5-methoxy-8-methyl-6-oxo-3,4-dihydro-2H,6H-pyrano[3,2-g]chromene-3-carboxylic acid amide

Guidance literature:: Multi-step reaction with 2 steps

1: 116 percent / 10percent NaOH / ethanol / 12 h / Ambient temperature

2: 56.4 percent / piperidine / ethanol / 30 h / Heating

With piperidine; sodium hydroxide; In ethanol;