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(S)-4,5-dihydro-2-[2-hydroxy-4-[12-(tert-butoxycarbonylamino)-5,9-bis(tert-butoxycarbonyl)-5,9-diazadodecyloxy]phenyl]-4-methyl-4-thiazolecarboxylic acid

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  • Chemical Name:(S)-4,5-dihydro-2-[2-hydroxy-4-[12-(tert-butoxycarbonylamino)-5,9-bis(tert-butoxycarbonyl)-5,9-diazadodecyloxy]phenyl]-4-methyl-4-thiazolecarboxylic acid
  • CAS No.:847829-20-3
  • Molecular Formula:C36H58N4O10S
  • Molecular Weight:738.943
  • Hs Code.:
(S)-4,5-dihydro-2-[2-hydroxy-4-[12-(tert-butoxycarbonylamino)-5,9-bis(tert-butoxycarbonyl)-5,9-diazadodecyloxy]phenyl]-4-methyl-4-thiazolecarboxylic acid

Synonyms:(S)-4,5-dihydro-2-[2-hydroxy-4-[12-(tert-butoxycarbonylamino)-5,9-bis(tert-butoxycarbonyl)-5,9-diazadodecyloxy]phenyl]-4-methyl-4-thiazolecarboxylic acid

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Chemical Property of (S)-4,5-dihydro-2-[2-hydroxy-4-[12-(tert-butoxycarbonylamino)-5,9-bis(tert-butoxycarbonyl)-5,9-diazadodecyloxy]phenyl]-4-methyl-4-thiazolecarboxylic acid
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Technology Process of (S)-4,5-dihydro-2-[2-hydroxy-4-[12-(tert-butoxycarbonylamino)-5,9-bis(tert-butoxycarbonyl)-5,9-diazadodecyloxy]phenyl]-4-methyl-4-thiazolecarboxylic acid

There total 11 articles about (S)-4,5-dihydro-2-[2-hydroxy-4-[12-(tert-butoxycarbonylamino)-5,9-bis(tert-butoxycarbonyl)-5,9-diazadodecyloxy]phenyl]-4-methyl-4-thiazolecarboxylic acid 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 8 steps
1.1: aq. NaOH; H2 / Raney Ni / ethanol / 12 h / 2585.74 - 2844.31 Torr
2.1: 11.38 g / CH2Cl2; H2O / 12 h / 20 °C
3.1: sodium hydride / dimethylformamide / 1.75 h / 0 - 20 °C
3.2: 78 percent / dimethylformamide / 19 h
4.1: HBr; AcOH; phenol / CH2Cl2 / 12 h / 0 °C
5.1: 2.46 g / triethylamine / tetrahydrofuran; H2O / 12 h / 20 °C
6.1: 92 percent / triethylamine / CH2Cl2 / 12 h / 20 °C
7.1: 67 percent / NaOEt / ethanol / 15 h / 60 °C
8.1: 63 percent / NaOH / methanol / 15 h / 20 °C
With sodium hydroxide; hydrogen bromide; hydrogen; sodium ethanolate; sodium hydride; acetic acid; triethylamine; phenol; nickel; In tetrahydrofuran; methanol; ethanol; dichloromethane; water; N,N-dimethyl-formamide;
DOI:10.1021/jm048974f
Guidance literature:
Multi-step reaction with 2 steps
1: 67 percent / NaOEt / ethanol / 15 h / 60 °C
2: 63 percent / NaOH / methanol / 15 h / 20 °C
With sodium hydroxide; sodium ethanolate; In methanol; ethanol;
DOI:10.1021/jm048974f
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