5-(benzyloxy)-2-(3,4-bis(benzyloxy)phenyl)-7-morpholino-4H-chromen-4-one

Base Information

Chemical Name:5-(benzyloxy)-2-(3,4-bis(benzyloxy)phenyl)-7-morpholino-4H-chromen-4-one
CAS No.:1610737-94-4
Molecular Formula:C₄₀H₃₅NO₆
Molecular Weight:625.721
Hs Code.:

Synonyms:5-(benzyloxy)-2-(3,4-bis(benzyloxy)phenyl)-7-morpholino-4H-chromen-4-one

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Chemical Property of 5-(benzyloxy)-2-(3,4-bis(benzyloxy)phenyl)-7-morpholino-4H-chromen-4-one

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Technology Process of 5-(benzyloxy)-2-(3,4-bis(benzyloxy)phenyl)-7-morpholino-4H-chromen-4-one

There total 6 articles about 5-(benzyloxy)-2-(3,4-bis(benzyloxy)phenyl)-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:

: 110-91-8,99108-56-2
morpholine

: 1610737-90-0
5-(benzyloxy)-2-(3,4-bis(benzyloxy)phenyl)-4-oxo-4H-chromen-7-yl-4-methylbenzenesulfonate

: 1610737-94-4
5-(benzyloxy)-2-(3,4-bis(benzyloxy)phenyl)-7-morpholino-4H-chromen-4-one

Guidance literature:: With palladium diacetate; caesium carbonate; XPhos; In 1,4-dioxane; at 110 ℃; for 3h; Microwave irradiation;
DOI:10.1016/j.bmc.2014.04.016

Reference yield:

: 1610737-84-2
4-(5-acetoxy-4-oxo-7-(tosyloxy)-4H-chromen-2-yl)-1,2-phenylene diacetate

: 1610737-94-4
5-(benzyloxy)-2-(3,4-bis(benzyloxy)phenyl)-7-morpholino-4H-chromen-4-one

Guidance literature:: Multi-step reaction with 3 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

With ammonia; 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:

: 1061-93-4
luteolin tetraacetate

: 1610737-94-4
5-(benzyloxy)-2-(3,4-bis(benzyloxy)phenyl)-7-morpholino-4H-chromen-4-one

Guidance literature:: Multi-step reaction with 5 steps

1: thiophenol; 1H-imidazole / 1-methyl-pyrrolidin-2-one / 2 h / 0 - 20 °C

2: triethylamine / tetrahydrofuran / 8 h / 20 °C

3: ammonia / methanol / 2 h / 20 °C

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

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

With 1H-imidazole; ammonia; palladium diacetate; potassium carbonate; caesium carbonate; thiophenol; triethylamine; XPhos; In tetrahydrofuran; 1,4-dioxane; 1-methyl-pyrrolidin-2-one; methanol; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2014.04.016