2-benzenesulfonylamino-3-[(2-phenylamino-3H-benzoimidazole-5-carbonyl)-amino]-propionic acid tert-butyl ester

Base Information

Chemical Name:2-benzenesulfonylamino-3-[(2-phenylamino-3H-benzoimidazole-5-carbonyl)-amino]-propionic acid tert-butyl ester
CAS No.:215050-27-4
Molecular Formula:C₂₇H₂₉N₅O₅S
Molecular Weight:535.624
Hs Code.:

2-benzenesulfonylamino-3-[(2-phenylamino-3<i>H</i>-benzoimidazole-5-carbonyl)-amino]-propionic acid <i>tert</i>-butyl ester

Synonyms:2-benzenesulfonylamino-3-[(2-phenylamino-3H-benzoimidazole-5-carbonyl)-amino]-propionic acid tert-butyl ester

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Chemical Property of 2-benzenesulfonylamino-3-[(2-phenylamino-3H-benzoimidazole-5-carbonyl)-amino]-propionic acid tert-butyl ester

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Technology Process of 2-benzenesulfonylamino-3-[(2-phenylamino-3H-benzoimidazole-5-carbonyl)-amino]-propionic acid tert-butyl ester

There total 9 articles about 2-benzenesulfonylamino-3-[(2-phenylamino-3H-benzoimidazole-5-carbonyl)-amino]-propionic 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: 81.0%

: 215050-26-3
3-[4-amino-3-(3-phenyl-thioureido)-benzoylamino]-2-benzenesulfonylamino-propionic acid tert-butyl ester

: 215050-27-4
2-benzenesulfonylamino-3-[(2-phenylamino-3H-benzoimidazole-5-carbonyl)-amino]-propionic acid tert-butyl ester

Guidance literature:: With triethylamine; mercury dichloride; In N,N-dimethyl-formamide; at 25 ℃; for 4h;
DOI:10.1016/S0968-0896(98)00090-X

Reference yield:

: 453-71-4
3-nitro-4-fluorobenzoic acid

: 215050-27-4
2-benzenesulfonylamino-3-[(2-phenylamino-3H-benzoimidazole-5-carbonyl)-amino]-propionic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: 99 percent / (COCl)2 / dimethylformamide; benzene / 6 h / 0 °C

2: 98 percent / Et₃N / CH₂Cl₂ / 4 h / 0 °C

3: 93 percent / NH₃ / dimethylformamide / 5 h / 25 °C

4: 90 percent / H₂ / Pd-C / methanol / 8 h / 25 °C

5: 69 percent / Et₃N / ethanol / 14 h / 25 °C

6: 81 percent / Et₃N; HgCl₂ / dimethylformamide / 4 h / 25 °C

With oxalyl dichloride; ammonia; hydrogen; triethylamine; mercury dichloride; palladium on activated charcoal; In methanol; ethanol; dichloromethane; N,N-dimethyl-formamide; benzene; 1: Chlorination / 2: Acylation / 3: Substitution / 4: Hydrogenation / 5: Substitution / 6: Cyclization;
DOI:10.1016/S0968-0896(98)00090-X

Reference yield:

: 400-94-2
4-fluoro-3-nitrobenzoyl chloride

: 215050-27-4
2-benzenesulfonylamino-3-[(2-phenylamino-3H-benzoimidazole-5-carbonyl)-amino]-propionic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 98 percent / Et₃N / CH₂Cl₂ / 4 h / 0 °C

2: 93 percent / NH₃ / dimethylformamide / 5 h / 25 °C

3: 90 percent / H₂ / Pd-C / methanol / 8 h / 25 °C

4: 69 percent / Et₃N / ethanol / 14 h / 25 °C

5: 81 percent / Et₃N; HgCl₂ / dimethylformamide / 4 h / 25 °C

With ammonia; hydrogen; triethylamine; mercury dichloride; palladium on activated charcoal; In methanol; ethanol; dichloromethane; N,N-dimethyl-formamide; 1: Acylation / 2: Substitution / 3: Hydrogenation / 4: Substitution / 5: Cyclization;
DOI:10.1016/S0968-0896(98)00090-X