2-(3,4-dihydroxyphenyl)-5-hydroxy-7-morpholino-4H-chromen-4-one

Base Information

• Chemical Name: 2-(3,4-dihydroxyphenyl)-5-hydroxy-7-morpholino-4H-chromen-4-one
• CAS No.: 1610737-73-9
• Molecular Formula: C₁₉H₁₇NO₆
• Molecular Weight: 355.347
• Mol file: 1610737-73-9.mol

Synonyms:2-(3,4-dihydroxyphenyl)-5-hydroxy-7-morpholino-4H-chromen-4-one

Chemical Property of 2-(3,4-dihydroxyphenyl)-5-hydroxy-7-morpholino-4H-chromen-4-one

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 2-(3,4-dihydroxyphenyl)-5-hydroxy-7-morpholino-4H-chromen-4-one

There total 7 articles about 2-(3,4-dihydroxyphenyl)-5-hydroxy-7-morpholino-4H-chromen-4-one 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: 60.0%

5-(benzyloxy)-2-(3,4-bis(benzyloxy)phenyl)-7-morpholino-4H-chromen-4-one (1610737-94-4) → 2-(3,4-dihydroxyphenyl)-5-hydroxy-7-morpholino-4H-chromen-4-one (1610737-73-9)

Guidance literature:

With 10% Pd(OH)2/C; hydrogen; In methanol;

DOI:10.1016/j.bmc.2014.04.016

Reference yield:

4-(5-acetoxy-4-oxo-7-(tosyloxy)-4H-chromen-2-yl)-1,2-phenylene diacetate (1610737-84-2) → 2-(3,4-dihydroxyphenyl)-5-hydroxy-7-morpholino-4H-chromen-4-one (1610737-73-9)

Guidance literature:

Multi-step reaction with 4 steps

1: ammonia / methanol / 2 h / 20 °C

2: potassium carbonate / N,N-dimethyl-formamide / 12 h / 20 °C / Inert atmosphere

3: palladium diacetate; XPhos; caesium carbonate / 1,4-dioxane / 3 h / 110 °C / Microwave irradiation

4: 10% Pd(OH)2/C; hydrogen / methanol

With 10% Pd(OH)2/C; ammonia; hydrogen; palladium diacetate; potassium carbonate; caesium carbonate; XPhos; In 1,4-dioxane; methanol; N,N-dimethyl-formamide;

DOI:10.1016/j.bmc.2014.04.016

Reference yield:

2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxo-4H-chromen-7-yl-4-methylbenzenesulfonate (1610737-88-6) → 2-(3,4-dihydroxyphenyl)-5-hydroxy-7-morpholino-4H-chromen-4-one (1610737-73-9)

Guidance literature:

Multi-step reaction with 3 steps

1: potassium carbonate / N,N-dimethyl-formamide / 12 h / 20 °C / Inert atmosphere

2: palladium diacetate; XPhos; caesium carbonate / 1,4-dioxane / 3 h / 110 °C / Microwave irradiation

3: 10% Pd(OH)2/C; hydrogen / methanol

With 10% Pd(OH)2/C; hydrogen; palladium diacetate; potassium carbonate; caesium carbonate; XPhos; In 1,4-dioxane; methanol; N,N-dimethyl-formamide;

DOI:10.1016/j.bmc.2014.04.016

upstream raw materials:

luteolin tetraacetate

4-(5-acetoxy-4-oxo-7-(tosyloxy)-4H-chromen-2-yl)-1,2-phenylene diacetate

2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxo-4H-chromen-7-yl-4-methylbenzenesulfonate

5-(benzyloxy)-2-(3,4-bis(benzyloxy)phenyl)-4-oxo-4H-chromen-7-yl-4-methylbenzenesulfonate