benzyl 2-(benzyloxy)-4-(2-(N,4-dimethylphenylsulfonamido)-N-(4-(1-(2,2,2-trifluoroacetyl)piperidin-4-yl)benzyl)acetamido)benzoate

Base Information

Chemical Name:benzyl 2-(benzyloxy)-4-(2-(N,4-dimethylphenylsulfonamido)-N-(4-(1-(2,2,2-trifluoroacetyl)piperidin-4-yl)benzyl)acetamido)benzoate
CAS No.:1331747-81-9
Molecular Formula:C₄₅H₄₄F₃N₃O₇S
Molecular Weight:827.921
Hs Code.:

Synonyms:benzyl 2-(benzyloxy)-4-(2-(N,4-dimethylphenylsulfonamido)-N-(4-(1-(2,2,2-trifluoroacetyl)piperidin-4-yl)benzyl)acetamido)benzoate

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Chemical Property of benzyl 2-(benzyloxy)-4-(2-(N,4-dimethylphenylsulfonamido)-N-(4-(1-(2,2,2-trifluoroacetyl)piperidin-4-yl)benzyl)acetamido)benzoate

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Technology Process of benzyl 2-(benzyloxy)-4-(2-(N,4-dimethylphenylsulfonamido)-N-(4-(1-(2,2,2-trifluoroacetyl)piperidin-4-yl)benzyl)acetamido)benzoate

There total 11 articles about benzyl 2-(benzyloxy)-4-(2-(N,4-dimethylphenylsulfonamido)-N-(4-(1-(2,2,2-trifluoroacetyl)piperidin-4-yl)benzyl)acetamido)benzoate 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:

: C₃₅H₃₃F₃N₂O₄

: 2644-99-7
2-(N-methyl-N-(p-toluenesulfonamido))acetic acid

: 1331747-81-9
benzyl 2-(benzyloxy)-4-(2-(N,4-dimethylphenylsulfonamido)-N-(4-(1-(2,2,2-trifluoroacetyl)piperidin-4-yl)benzyl)acetamido)benzoate

Guidance literature:: With dichlorotriphenylphosphorane; In chloroform; at 60 ℃; for 12h; Inert atmosphere;
DOI:10.1002/cmdc.201100194

Reference yield:

: 771-99-3
4-phenylpiperidine

: 1331747-81-9
benzyl 2-(benzyloxy)-4-(2-(N,4-dimethylphenylsulfonamido)-N-(4-(1-(2,2,2-trifluoroacetyl)piperidin-4-yl)benzyl)acetamido)benzoate

Guidance literature:: Multi-step reaction with 5 steps

1.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 3 h / 0 - 20 °C / Inert atmosphere

2.1: aluminum (III) chloride / dichloromethane / 1 h / 0 °C / Inert atmosphere

3.1: palladium 10% on activated carbon; hydrogen; N-ethyl-N,N-diisopropylamine / ethyl acetate / 2 h / 20 °C

4.1: acetic acid / methanol / 3 h / 45 °C / Molecular sieve; Inert atmosphere

4.2: 12 h / 20 °C / Inert atmosphere

5.1: dichlorotriphenylphosphorane / chloroform / 12 h / 60 °C / Inert atmosphere

With aluminum (III) chloride; palladium 10% on activated carbon; hydrogen; acetic acid; N-ethyl-N,N-diisopropylamine; dichlorotriphenylphosphorane; In methanol; dichloromethane; chloroform; ethyl acetate; 2.1: Friedel Crafts acylation / 3.1: Rosenmund reduction;
DOI:10.1002/cmdc.201100194

Reference yield:

: 1241832-99-4
benzyl 4-amino-2-(benzyloxy)benzoate

: 1331747-81-9
benzyl 2-(benzyloxy)-4-(2-(N,4-dimethylphenylsulfonamido)-N-(4-(1-(2,2,2-trifluoroacetyl)piperidin-4-yl)benzyl)acetamido)benzoate

Guidance literature:: Multi-step reaction with 2 steps

1.1: acetic acid / methanol / 3 h / 45 °C / Molecular sieve; Inert atmosphere

1.2: 12 h / 20 °C / Inert atmosphere

2.1: dichlorotriphenylphosphorane / chloroform / 12 h / 60 °C / Inert atmosphere

With acetic acid; dichlorotriphenylphosphorane; In methanol; chloroform;
DOI:10.1002/cmdc.201100194