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cyclo-3-bromo-4-O-methyl-L-tyrosyl-L-tyrosine

Base Information
  • Chemical Name:cyclo-3-bromo-4-O-methyl-L-tyrosyl-L-tyrosine
  • CAS No.:98778-76-8
  • Molecular Formula:C19H19BrN2O4
  • Molecular Weight:419.275
  • Hs Code.:
cyclo-3-bromo-4-O-methyl-L-tyrosyl-L-tyrosine

Synonyms:

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Chemical Property of cyclo-3-bromo-4-O-methyl-L-tyrosyl-L-tyrosine
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Technology Process of cyclo-3-bromo-4-O-methyl-L-tyrosyl-L-tyrosine

There total 5 articles about cyclo-3-bromo-4-O-methyl-L-tyrosyl-L-tyrosine 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 4 steps
1: 1.) Br2, 98percent formic acid, 2.) 3N aq. HCl / 1.) 6 h, 2.) reflux, 1 h
2: 92 percent / thionyl chloride / 3 h / Heating
3: 87 percent / triethylamine, dicyclohexylcarbodiimide / dimethylformamide / 2 h / 0 °C
4: 1.) 98percent formic acid / 1.) 25 deg C, 2.) 2-BuOH, reflux
With hydrogenchloride; formic acid; thionyl chloride; bromine; triethylamine; dicyclohexyl-carbodiimide; In N,N-dimethyl-formamide;
DOI:10.1021/jo00224a051
Guidance literature:
Multi-step reaction with 2 steps
1: 87 percent / triethylamine, dicyclohexylcarbodiimide / dimethylformamide / 2 h / 0 °C
2: 1.) 98percent formic acid / 1.) 25 deg C, 2.) 2-BuOH, reflux
With formic acid; triethylamine; dicyclohexyl-carbodiimide; In N,N-dimethyl-formamide;
DOI:10.1021/jo00224a051
Guidance literature:
Multi-step reaction with 3 steps
1: 92 percent / thionyl chloride / 3 h / Heating
2: 87 percent / triethylamine, dicyclohexylcarbodiimide / dimethylformamide / 2 h / 0 °C
3: 1.) 98percent formic acid / 1.) 25 deg C, 2.) 2-BuOH, reflux
With formic acid; thionyl chloride; triethylamine; dicyclohexyl-carbodiimide; In N,N-dimethyl-formamide;
DOI:10.1021/jo00224a051
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