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(2S,8S,E)-benzyl 8-(tert-butoxycarbonylamino)-2-(dibenzylamino)-7-oxonon-5-enoate

Base Information
  • Chemical Name:(2S,8S,E)-benzyl 8-(tert-butoxycarbonylamino)-2-(dibenzylamino)-7-oxonon-5-enoate
  • CAS No.:1379764-47-2
  • Molecular Formula:C35H42N2O5
  • Molecular Weight:570.729
  • Hs Code.:
(2S,8S,E)-benzyl 8-(tert-butoxycarbonylamino)-2-(dibenzylamino)-7-oxonon-5-enoate

Synonyms:(2S,8S,E)-benzyl 8-(tert-butoxycarbonylamino)-2-(dibenzylamino)-7-oxonon-5-enoate

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Chemical Property of (2S,8S,E)-benzyl 8-(tert-butoxycarbonylamino)-2-(dibenzylamino)-7-oxonon-5-enoate
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Technology Process of (2S,8S,E)-benzyl 8-(tert-butoxycarbonylamino)-2-(dibenzylamino)-7-oxonon-5-enoate

There total 2 articles about (2S,8S,E)-benzyl 8-(tert-butoxycarbonylamino)-2-(dibenzylamino)-7-oxonon-5-enoate 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:
dimethyl (S)-3-[N-(tert-butoxycarbonyl)amino]-2-oxobutylphosphonate; With N-ethyl-N,N-diisopropylamine; lithium chloride; In acetonitrile; at 20 ℃; Inert atmosphere;
2-dibenzylamino-5-oxo-pentanoic acid benzyl ester; In acetonitrile; at 20 ℃; Inert atmosphere;
DOI:10.1002/ejoc.201101387
Guidance literature:
Multi-step reaction with 2 steps
1.1: n-butyllithium / tetrahydrofuran / -78 °C / Inert atmosphere
1.2: Inert atmosphere
2.1: N-ethyl-N,N-diisopropylamine; lithium chloride / acetonitrile / 20 °C / Inert atmosphere
2.2: 20 °C / Inert atmosphere
With n-butyllithium; N-ethyl-N,N-diisopropylamine; lithium chloride; In tetrahydrofuran; acetonitrile; 2.1: Horner-Wadsworth-Emmons olefination / 2.2: Horner-Wadsworth-Emmons olefination;
DOI:10.1002/ejoc.201101387
Guidance literature:
Multi-step reaction with 5 steps
1.1: 20% palladium hydroxide on charcoal; hydrogen; acetic acid / methanol / 8 h / 20 °C / 4560.31 Torr / Microwave irradiation
2.1: sodium hydroxide / tetrahydrofuran; water / 1 h / -5 - 20 °C
3.1: triethylsilane; trifluoroacetic acid / dichloromethane / 3 h / 20 °C / Inert atmosphere
4.1: triethylamine / water; acetonitrile / 1 h
5.1: 4-methyl-morpholine; benzotriazol-1-ol; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate / N,N-dimethyl-formamide / 2 h / 20 °C / Inert atmosphere; solid phase reaction
5.2: 0.17 h / Inert atmosphere; solid phase reaction
With 4-methyl-morpholine; triethylsilane; 20% palladium hydroxide on charcoal; hydrogen; benzotriazol-1-ol; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; acetic acid; triethylamine; trifluoroacetic acid; sodium hydroxide; In tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1002/ejoc.201101387
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