N-(5-amino-2-oxo-2,3-dihydro-benzoxazol-6-yl)-2-(4-benzylpiperidin-1-yl)-2-oxo-acetamide

Base Information

Chemical Name:N-(5-amino-2-oxo-2,3-dihydro-benzoxazol-6-yl)-2-(4-benzylpiperidin-1-yl)-2-oxo-acetamide
CAS No.:933474-46-5
Molecular Formula:C₂₁H₂₂N₄O₄
Molecular Weight:394.43
Hs Code.:

Synonyms:N-(5-amino-2-oxo-2,3-dihydro-benzoxazol-6-yl)-2-(4-benzylpiperidin-1-yl)-2-oxo-acetamide

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Chemical Property of N-(5-amino-2-oxo-2,3-dihydro-benzoxazol-6-yl)-2-(4-benzylpiperidin-1-yl)-2-oxo-acetamide

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Technology Process of N-(5-amino-2-oxo-2,3-dihydro-benzoxazol-6-yl)-2-(4-benzylpiperidin-1-yl)-2-oxo-acetamide

There total 8 articles about N-(5-amino-2-oxo-2,3-dihydro-benzoxazol-6-yl)-2-(4-benzylpiperidin-1-yl)-2-oxo-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: 34.5%

: 933474-45-4
2-(4-benzylpiperidin-1-yl)-N-(5-nitro-2-oxo-2,3-dihydro-benzoxazol-6-yl)-2-oxo-acetamide

: 933474-46-5
N-(5-amino-2-oxo-2,3-dihydro-benzoxazol-6-yl)-2-(4-benzylpiperidin-1-yl)-2-oxo-acetamide

Guidance literature:: With hydrogen; palladium on activated charcoal; In methanol; for 8h;
DOI:10.1021/jm060420k

Reference yield:

: 31252-42-3
4-benzylpyperidine

: 933474-46-5
N-(5-amino-2-oxo-2,3-dihydro-benzoxazol-6-yl)-2-(4-benzylpiperidin-1-yl)-2-oxo-acetamide

Guidance literature:: Multi-step reaction with 5 steps

1: 99 percent / N-ethyldiisopropylamine / CH₂Cl₂ / 0.5 h / 0 °C

2: 85 percent / KOH / methanol / 6 h / 20 °C

3: 99.5 percent / thionyl chloride / 2 h / Heating

4: 47 percent / triethylamine / CHCl₃ / 2 h / 20 °C

5: 34.5 percent / H₂ / Pd/C / methanol / 8 h

With potassium hydroxide; thionyl chloride; hydrogen; triethylamine; N-ethyl-N,N-diisopropylamine; palladium on activated charcoal; In methanol; dichloromethane; chloroform;
DOI:10.1021/jm060420k

Reference yield:

: 22876-17-1
6-amino-1,3-benzoxazol-2-(3H)-one

: 933474-46-5
N-(5-amino-2-oxo-2,3-dihydro-benzoxazol-6-yl)-2-(4-benzylpiperidin-1-yl)-2-oxo-acetamide

Guidance literature:: Multi-step reaction with 3 steps

1: 96 percent / TFA; sodium nitrate / 20 °C

2: 47 percent / triethylamine / CHCl₃ / 2 h / 20 °C

3: 34.5 percent / H₂ / Pd/C / methanol / 8 h

With sodium nitrate; hydrogen; triethylamine; trifluoroacetic acid; palladium on activated charcoal; In methanol; chloroform;
DOI:10.1021/jm060420k