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

Base Information

Chemical Name:N-(2-methoxy-4-(7-oxo-4,5,6,7-tetrahydrobenzo[d]isoxazol-3-yl)phenyl)-N-(2-oxopropyl)formamide
CAS No.:1433663-73-0
Molecular Formula:C₁₈H₁₈N₂O₅
Molecular Weight:342.351
Hs Code.:

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

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Chemical Property of N-(2-methoxy-4-(7-oxo-4,5,6,7-tetrahydrobenzo[d]isoxazol-3-yl)phenyl)-N-(2-oxopropyl)formamide

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Technology Process of N-(2-methoxy-4-(7-oxo-4,5,6,7-tetrahydrobenzo[d]isoxazol-3-yl)phenyl)-N-(2-oxopropyl)formamide

There total 6 articles about N-(2-methoxy-4-(7-oxo-4,5,6,7-tetrahydrobenzo[d]isoxazol-3-yl)phenyl)-N-(2-oxopropyl)formamide 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: 54.0%

: 1433663-66-1
N-(2-methoxy-4-(7-oxo-4,5,6,7-tetrahydrobenzo[d]isoxazol-3-yl)phenyl)formamide

: 78-95-5
chloroacetone

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

Guidance literature:: With caesium carbonate; potassium iodide; at 55 ℃; Inert atmosphere;
DOI:10.1021/acsmedchemlett.7b00178

Reference yield:

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

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

Guidance literature:: Multi-step reaction with 6 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

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

Reference yield:

: 80410-57-7
3-methoxy-4-nitrobenzaldehyde

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

Guidance literature:: Multi-step reaction with 5 steps

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

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

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

4: acetic anhydride / 1 h / Cooling

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

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