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5-tert-butoxycarbonylamino-3'-[(5-tert-butoxycarbonylamino-3'-nitrobiphenyl-3-carbonyl)amino]biphenyl-3-carboxylic acid 2-trimethylsilanylethyl ester

Base Information
  • Chemical Name:5-tert-butoxycarbonylamino-3'-[(5-tert-butoxycarbonylamino-3'-nitrobiphenyl-3-carbonyl)amino]biphenyl-3-carboxylic acid 2-trimethylsilanylethyl ester
  • CAS No.:337973-09-8
  • Molecular Formula:C41H48N4O9Si
  • Molecular Weight:768.939
  • Hs Code.:
5-tert-butoxycarbonylamino-3'-[(5-tert-butoxycarbonylamino-3'-nitrobiphenyl-3-carbonyl)amino]biphenyl-3-carboxylic acid 2-trimethylsilanylethyl ester

Synonyms:5-tert-butoxycarbonylamino-3'-[(5-tert-butoxycarbonylamino-3'-nitrobiphenyl-3-carbonyl)amino]biphenyl-3-carboxylic acid 2-trimethylsilanylethyl ester

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Chemical Property of 5-tert-butoxycarbonylamino-3'-[(5-tert-butoxycarbonylamino-3'-nitrobiphenyl-3-carbonyl)amino]biphenyl-3-carboxylic acid 2-trimethylsilanylethyl ester
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Technology Process of 5-tert-butoxycarbonylamino-3'-[(5-tert-butoxycarbonylamino-3'-nitrobiphenyl-3-carbonyl)amino]biphenyl-3-carboxylic acid 2-trimethylsilanylethyl ester

There total 6 articles about 5-tert-butoxycarbonylamino-3'-[(5-tert-butoxycarbonylamino-3'-nitrobiphenyl-3-carbonyl)amino]biphenyl-3-carboxylic acid 2-trimethylsilanylethyl 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:
Guidance literature:
Multi-step reaction with 6 steps
1: 88 percent / (NH4)2Fe(SO4)2; aq. NH3 / 0.17 h / Heating
2: 1.04 g / dioxane; aq. KOH
3: 83 percent / aq. Na2CO3; Pd(OAc)2 / dimethylformamide / 4 h / 80 °C
4: DMAP; DCC / CH2Cl2; tetrahydrofuran
5: H2 / Pd/C / methanol; ethyl acetate / 2068.59 Torr
6: bis(2-oxo-3-oxazolidinyl)phosphinic chloride; DIEA / tetrahydrofuran
With dmap; palladium diacetate; ammonium iron (II) sulfate; ammonium hydroxide; hydrogen; bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride; sodium carbonate; N-ethyl-N,N-diisopropylamine; dicyclohexyl-carbodiimide; palladium on activated charcoal; In tetrahydrofuran; 1,4-dioxane; methanol; potassium hydroxide; dichloromethane; ethyl acetate; N,N-dimethyl-formamide; 3: Suzuki coupling;
DOI:10.1021/ja034563x
Guidance literature:
Multi-step reaction with 4 steps
1: 83 percent / aq. Na2CO3; Pd(OAc)2 / dimethylformamide / 4 h / 80 °C
2: DMAP; DCC / CH2Cl2; tetrahydrofuran
3: H2 / Pd/C / methanol; ethyl acetate / 2068.59 Torr
4: bis(2-oxo-3-oxazolidinyl)phosphinic chloride; DIEA / tetrahydrofuran
With dmap; palladium diacetate; hydrogen; bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride; sodium carbonate; N-ethyl-N,N-diisopropylamine; dicyclohexyl-carbodiimide; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane; ethyl acetate; N,N-dimethyl-formamide; 1: Suzuki coupling;
DOI:10.1021/ja034563x
Guidance literature:
Multi-step reaction with 5 steps
1: 1.04 g / dioxane; aq. KOH
2: 83 percent / aq. Na2CO3; Pd(OAc)2 / dimethylformamide / 4 h / 80 °C
3: DMAP; DCC / CH2Cl2; tetrahydrofuran
4: H2 / Pd/C / methanol; ethyl acetate / 2068.59 Torr
5: bis(2-oxo-3-oxazolidinyl)phosphinic chloride; DIEA / tetrahydrofuran
With dmap; palladium diacetate; hydrogen; bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride; sodium carbonate; N-ethyl-N,N-diisopropylamine; dicyclohexyl-carbodiimide; palladium on activated charcoal; In tetrahydrofuran; 1,4-dioxane; methanol; potassium hydroxide; dichloromethane; ethyl acetate; N,N-dimethyl-formamide; 2: Suzuki coupling;
DOI:10.1021/ja034563x
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