2-(4-fluorophenyl)-N-(4-methoxybenzyl)-N-[1-(8-methyl-3-oxo-3,4-dihydro-2H-1,4-benzoxazin-6-yl)-1-oxopropan-2-yl]acetamide

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Chemical Name:2-(4-fluorophenyl)-N-(4-methoxybenzyl)-N-[1-(8-methyl-3-oxo-3,4-dihydro-2H-1,4-benzoxazin-6-yl)-1-oxopropan-2-yl]acetamide
CAS No.:1454580-40-5
Molecular Formula:C₂₈H₂₇FN₂O₅
Molecular Weight:490.531
Hs Code.:

Synonyms:2-(4-fluorophenyl)-N-(4-methoxybenzyl)-N-[1-(8-methyl-3-oxo-3,4-dihydro-2H-1,4-benzoxazin-6-yl)-1-oxopropan-2-yl]acetamide

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Chemical Property of 2-(4-fluorophenyl)-N-(4-methoxybenzyl)-N-[1-(8-methyl-3-oxo-3,4-dihydro-2H-1,4-benzoxazin-6-yl)-1-oxopropan-2-yl]acetamide

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Technology Process of 2-(4-fluorophenyl)-N-(4-methoxybenzyl)-N-[1-(8-methyl-3-oxo-3,4-dihydro-2H-1,4-benzoxazin-6-yl)-1-oxopropan-2-yl]acetamide

There total 5 articles about 2-(4-fluorophenyl)-N-(4-methoxybenzyl)-N-[1-(8-methyl-3-oxo-3,4-dihydro-2H-1,4-benzoxazin-6-yl)-1-oxopropan-2-yl]acetamide 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: 86.0%

: 1454580-34-7
6-{2-[(4-methoxybenzyl)amino]propanoyl}-8-methyl-2H-1,4-benzoxazin-3(4H)-one

: 459-04-1
4-Fluorophenylacetyl chloride

: 1454580-40-5
2-(4-fluorophenyl)-N-(4-methoxybenzyl)-N-[1-(8-methyl-3-oxo-3,4-dihydro-2H-1,4-benzoxazin-6-yl)-1-oxopropan-2-yl]acetamide

Guidance literature:: In tetrahydrofuran; water; at 0 - 20 ℃;
DOI:10.1016/j.bmc.2013.07.043

Reference yield:

: 1454580-28-9
8-methyl-6-propionyl-2H-1,4-benzoxazin-3(4H)-one

: 1454580-40-5
2-(4-fluorophenyl)-N-(4-methoxybenzyl)-N-[1-(8-methyl-3-oxo-3,4-dihydro-2H-1,4-benzoxazin-6-yl)-1-oxopropan-2-yl]acetamide

Guidance literature:: Multi-step reaction with 3 steps

1: hydrogen bromide; pyridinium hydrobromide perbromide / acetic acid / 3 h / 20 °C

2: triethylamine / tetrahydrofuran; water / 2 h / 50 °C

3: tetrahydrofuran; water / 0 - 20 °C

With pyridinium hydrobromide perbromide; hydrogen bromide; triethylamine; In tetrahydrofuran; water; acetic acid;
DOI:10.1016/j.bmc.2013.07.043

Reference yield:

: 141771-81-5
1-(4-hydroxy-3-methyl-5-nitrophenyl)propan-1-one

: 1454580-40-5
2-(4-fluorophenyl)-N-(4-methoxybenzyl)-N-[1-(8-methyl-3-oxo-3,4-dihydro-2H-1,4-benzoxazin-6-yl)-1-oxopropan-2-yl]acetamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: zinc / 0.17 h

1.2: 14 h / 0 - 50 °C

2.1: hydrogen bromide; pyridinium hydrobromide perbromide / acetic acid / 3 h / 20 °C

3.1: triethylamine / tetrahydrofuran; water / 2 h / 50 °C

4.1: tetrahydrofuran; water / 0 - 20 °C

With pyridinium hydrobromide perbromide; hydrogen bromide; triethylamine; zinc; In tetrahydrofuran; water; acetic acid;
DOI:10.1016/j.bmc.2013.07.043