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(2S,11S,12R)-7-Benzenesulfonyl-12-isobutyl-13-oxo-1,7-diaza-cyclotridecane-2,11-dicarboxylic acid 11-(benzyloxy-amide) 2-methylamide

Base Information
  • Chemical Name:(2S,11S,12R)-7-Benzenesulfonyl-12-isobutyl-13-oxo-1,7-diaza-cyclotridecane-2,11-dicarboxylic acid 11-(benzyloxy-amide) 2-methylamide
  • CAS No.:191408-02-3
  • Molecular Formula:C31H44N4O6S
  • Molecular Weight:600.78
  • Hs Code.:
(2S,11S,12R)-7-Benzenesulfonyl-12-isobutyl-13-oxo-1,7-diaza-cyclotridecane-2,11-dicarboxylic acid 11-(benzyloxy-amide) 2-methylamide

Synonyms:(2S,11S,12R)-7-Benzenesulfonyl-12-isobutyl-13-oxo-1,7-diaza-cyclotridecane-2,11-dicarboxylic acid 11-(benzyloxy-amide) 2-methylamide

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Chemical Property of (2S,11S,12R)-7-Benzenesulfonyl-12-isobutyl-13-oxo-1,7-diaza-cyclotridecane-2,11-dicarboxylic acid 11-(benzyloxy-amide) 2-methylamide
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Technology Process of (2S,11S,12R)-7-Benzenesulfonyl-12-isobutyl-13-oxo-1,7-diaza-cyclotridecane-2,11-dicarboxylic acid 11-(benzyloxy-amide) 2-methylamide

There total 7 articles about (2S,11S,12R)-7-Benzenesulfonyl-12-isobutyl-13-oxo-1,7-diaza-cyclotridecane-2,11-dicarboxylic acid 11-(benzyloxy-amide) 2-methylamide 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 5 steps
1: H2 / Pd/C / methanol / 3 h
2: 90 percent / BOP; DIEA / dimethylformamide
3: 55 percent / DIAD; PPh3 / tetrahydrofuran
4: TFA / CH2Cl2
5: BOP; DIEA / dimethylformamide
With di-isopropyl azodicarboxylate; hydrogen; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine; triphenylphosphine; trifluoroacetic acid; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide; 3: Mitsunobu reaction;
DOI:10.1021/jm010127e
Guidance literature:
Multi-step reaction with 6 steps
1.1: 9-BBN / tetrahydrofuran / 12 h / 20 °C
1.2: 64 percent / aq. H2O2; AcONa / tetrahydrofuran / 0.33 h / 0 °C
2.1: H2 / Pd/C / methanol / 3 h
3.1: 90 percent / BOP; DIEA / dimethylformamide
4.1: 55 percent / DIAD; PPh3 / tetrahydrofuran
5.1: TFA / CH2Cl2
6.1: BOP; DIEA / dimethylformamide
With 9-borabicyclo[3.3.1]nonane dimer; di-isopropyl azodicarboxylate; hydrogen; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine; triphenylphosphine; trifluoroacetic acid; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide; 4.1: Mitsunobu reaction;
DOI:10.1021/jm010127e
Guidance literature:
Multi-step reaction with 7 steps
1.1: 62 percent / DBU / benzene / 4 h / Heating
2.1: 9-BBN / tetrahydrofuran / 12 h / 20 °C
2.2: 64 percent / aq. H2O2; AcONa / tetrahydrofuran / 0.33 h / 0 °C
3.1: H2 / Pd/C / methanol / 3 h
4.1: 90 percent / BOP; DIEA / dimethylformamide
5.1: 55 percent / DIAD; PPh3 / tetrahydrofuran
6.1: TFA / CH2Cl2
7.1: BOP; DIEA / dimethylformamide
With 9-borabicyclo[3.3.1]nonane dimer; di-isopropyl azodicarboxylate; hydrogen; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; 1,8-diazabicyclo[5.4.0]undec-7-ene; N-ethyl-N,N-diisopropylamine; triphenylphosphine; trifluoroacetic acid; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide; benzene; 5.1: Mitsunobu reaction;
DOI:10.1021/jm010127e
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