[2-Oxo-5-phenyl-3-(toluene-4-sulfonylamino)-2,3-dihydro-benzo[e][1,4]diazepin-1-yl]-acetic acid tert-butyl ester

Base Information

• Chemical Name: [2-Oxo-5-phenyl-3-(toluene-4-sulfonylamino)-2,3-dihydro-benzo[e][1,4]diazepin-1-yl]-acetic acid tert-butyl ester
• CAS No.: 215511-38-9
• Molecular Formula: C₂₈H₂₉N₃O₅S
• Molecular Weight: 519.621

Synonyms:[2-Oxo-5-phenyl-3-(toluene-4-sulfonylamino)-2,3-dihydro-benzo[e][1,4]diazepin-1-yl]-acetic acid tert-butyl ester

Chemical Property of [2-Oxo-5-phenyl-3-(toluene-4-sulfonylamino)-2,3-dihydro-benzo[e][1,4]diazepin-1-yl]-acetic acid tert-butyl ester

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Technology Process of [2-Oxo-5-phenyl-3-(toluene-4-sulfonylamino)-2,3-dihydro-benzo[e][1,4]diazepin-1-yl]-acetic acid tert-butyl ester

There total 3 articles about [2-Oxo-5-phenyl-3-(toluene-4-sulfonylamino)-2,3-dihydro-benzo[e][1,4]diazepin-1-yl]-acetic acid tert-butyl ester 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: 58.0%

bromoacetic acid tert-butyl ester (5292-43-3) + 4-Methyl-N-(2-oxo-5-phenyl-2,3-dihydro-1H-benzo[e][1,4]diazepin-3-yl)-benzenesulfonamide (215511-32-3) → [2-Oxo-5-phenyl-3-(toluene-4-sulfonylamino)-2,3-dihydro-benzo[e][1,4]diazepin-1-yl]-acetic acid tert-butyl ester (215511-38-9)

Guidance literature:

With sodium hydride; In N,N-dimethyl-formamide; at 20 ℃; for 1h;

DOI:10.1016/S0223-5234(98)80048-2

Reference yield:

p-toluenesulfonyl chloride (98-59-9) → [2-Oxo-5-phenyl-3-(toluene-4-sulfonylamino)-2,3-dihydro-benzo[e][1,4]diazepin-1-yl]-acetic acid tert-butyl ester (215511-38-9)

Guidance literature:

Multi-step reaction with 2 steps

1: 66 percent / NEt₃ / CHCl₃ / 0.5 h / Heating

2: 58 percent / NaH / dimethylformamide / 1 h / 20 °C

With sodium hydride; triethylamine; In chloroform; N,N-dimethyl-formamide;

DOI:10.1016/S0223-5234(98)80048-2

Reference yield:

3-amino-5-phenyl-1,3-dihydrobenzo[e][1,4]diazepin-2-one (103343-47-1) → [2-Oxo-5-phenyl-3-(toluene-4-sulfonylamino)-2,3-dihydro-benzo[e][1,4]diazepin-1-yl]-acetic acid tert-butyl ester (215511-38-9)

Guidance literature:

Multi-step reaction with 2 steps

1: 66 percent / NEt₃ / CHCl₃ / 0.5 h / Heating

2: 58 percent / NaH / dimethylformamide / 1 h / 20 °C

With sodium hydride; triethylamine; In chloroform; N,N-dimethyl-formamide;

DOI:10.1016/S0223-5234(98)80048-2

upstream raw materials:

bromoacetic acid tert-butyl ester

4-Methyl-N-(2-oxo-5-phenyl-2,3-dihydro-1H-benzo[e][1,4]diazepin-3-yl)-benzenesulfonamide

p-toluenesulfonyl chloride

3-amino-5-phenyl-1,3-dihydrobenzo[e][1,4]diazepin-2-one

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