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(S)-2-((S)-2-tert-Butoxycarbonylamino-propionylamino)-pentanedioic acid 1-allyl ester 5-[bis-(4-fluoro-phenyl)-pentafluorophenyl-methyl] ester

Base Information Edit
  • Chemical Name:(S)-2-((S)-2-tert-Butoxycarbonylamino-propionylamino)-pentanedioic acid 1-allyl ester 5-[bis-(4-fluoro-phenyl)-pentafluorophenyl-methyl] ester
  • CAS No.:241824-04-4
  • Molecular Formula:C35H33F7N2O7
  • Molecular Weight:726.645
  • Hs Code.:
  • Mol file:241824-04-4.mol
(S)-2-((S)-2-tert-Butoxycarbonylamino-propionylamino)-pentanedioic acid 1-allyl ester 5-[bis-(4-fluoro-phenyl)-pentafluorophenyl-methyl] ester

Synonyms:

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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of (S)-2-((S)-2-tert-Butoxycarbonylamino-propionylamino)-pentanedioic acid 1-allyl ester 5-[bis-(4-fluoro-phenyl)-pentafluorophenyl-methyl] ester Edit
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Technology Process of (S)-2-((S)-2-tert-Butoxycarbonylamino-propionylamino)-pentanedioic acid 1-allyl ester 5-[bis-(4-fluoro-phenyl)-pentafluorophenyl-methyl] ester

There total 7 articles about (S)-2-((S)-2-tert-Butoxycarbonylamino-propionylamino)-pentanedioic acid 1-allyl ester 5-[bis-(4-fluoro-phenyl)-pentafluorophenyl-methyl] 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 5 steps
1.1: Mg / diethyl ether
1.2: 94 percent / diethyl ether / 3 h / Heating
2.1: 100 percent / SOCl2 / 0.17 h / 20 °C
3.1: 84 percent / DIPEA / CH2Cl2 / 14 h / 20 °C
4.1: morpholie / dimethylformamide
5.1: 52 percent / coupling reagent
With morpholine; thionyl chloride; coupling reagent; magnesium; N-ethyl-N,N-diisopropylamine; In diethyl ether; dichloromethane; N,N-dimethyl-formamide; 1.1: Metallation / 1.2: Grignard reaction / 2.1: Substitution / 3.1: Alkylation / 4.1: Deacylation / 5.1: Acylation;
Guidance literature:
Multi-step reaction with 5 steps
1.1: Mg / diethyl ether
1.2: 94 percent / diethyl ether / 3 h / Heating
2.1: 100 percent / SOCl2 / 0.17 h / 20 °C
3.1: 84 percent / DIPEA / CH2Cl2 / 14 h / 20 °C
4.1: morpholie / dimethylformamide
5.1: 52 percent / coupling reagent
With morpholine; thionyl chloride; coupling reagent; magnesium; N-ethyl-N,N-diisopropylamine; In diethyl ether; dichloromethane; N,N-dimethyl-formamide; 1.1: Metallation / 1.2: Grignard reaction / 2.1: Substitution / 3.1: Alkylation / 4.1: Deacylation / 5.1: Acylation;
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