3-(3-methoxy-4-(4-methyl-1H-imidazol-1-yl)phenyl)-5,6-dihydrobenzo[d]isoxazol-7(4H)-one

Base Information

Chemical Name:3-(3-methoxy-4-(4-methyl-1H-imidazol-1-yl)phenyl)-5,6-dihydrobenzo[d]isoxazol-7(4H)-one
CAS No.:1433663-77-4
Molecular Formula:C₁₈H₁₇N₃O₃
Molecular Weight:323.351
Hs Code.:

Synonyms:3-(3-methoxy-4-(4-methyl-1H-imidazol-1-yl)phenyl)-5,6-dihydrobenzo[d]isoxazol-7(4H)-one

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Chemical Property of 3-(3-methoxy-4-(4-methyl-1H-imidazol-1-yl)phenyl)-5,6-dihydrobenzo[d]isoxazol-7(4H)-one

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Technology Process of 3-(3-methoxy-4-(4-methyl-1H-imidazol-1-yl)phenyl)-5,6-dihydrobenzo[d]isoxazol-7(4H)-one

There total 8 articles about 3-(3-methoxy-4-(4-methyl-1H-imidazol-1-yl)phenyl)-5,6-dihydrobenzo[d]isoxazol-7(4H)-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: 59.0%

: 1433663-73-0
N-(2-methoxy-4-(7-oxo-4,5,6,7-tetrahydrobenzo[d]isoxazol-3-yl)phenyl)-N-(2-oxopropyl)formamide

: 1433663-77-4
3-(3-methoxy-4-(4-methyl-1H-imidazol-1-yl)phenyl)-5,6-dihydrobenzo[d]isoxazol-7(4H)-one

Guidance literature:: With ammonium acetate; acetic acid; at 95 ℃; Inert atmosphere;
DOI:10.1021/acsmedchemlett.7b00178

Reference yield:

: 92206-38-7
ammonium acetate

: 1433663-73-0
N-(2-methoxy-4-(7-oxo-4,5,6,7-tetrahydrobenzo[d]isoxazol-3-yl)phenyl)-N-(2-oxopropyl)formamide

: 1433663-77-4
3-(3-methoxy-4-(4-methyl-1H-imidazol-1-yl)phenyl)-5,6-dihydrobenzo[d]isoxazol-7(4H)-one

Guidance literature:: With acetic acid; at 95 ℃; Inert atmosphere;

Reference yield:

: 704-13-2
5-formyl-2-nitrophenol

: 1433663-77-4
3-(3-methoxy-4-(4-methyl-1H-imidazol-1-yl)phenyl)-5,6-dihydrobenzo[d]isoxazol-7(4H)-one

Guidance literature:: Multi-step reaction with 7 steps

1: potassium carbonate / N,N-dimethyl-formamide

2: hydroxylamine hydrochloride / ethanol; water / 20 °C

3: N-chloro-succinimide / N,N-dimethyl-formamide / 15.25 h / 0 - 20 °C

4: tin(ll) chloride; ethanol / 2 h / 20 - 55 °C

5: acetic anhydride / 1 h / Cooling

6: caesium carbonate; potassium iodide / N,N-dimethyl-formamide; acetone / 55 °C

7: acetic acid / 95 °C / Inert atmosphere

With N-chloro-succinimide; ethanol; hydroxylamine hydrochloride; acetic anhydride; potassium carbonate; caesium carbonate; acetic acid; potassium iodide; tin(ll) chloride; In ethanol; water; N,N-dimethyl-formamide; acetone;