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(S)-N-(6-(1-amino-2-(3,5-difluorophenyl)ethyl)-2,5-dibromopyridin-3-yl)-2,2,2-trifluoroacetamide TFA salt

Base Information Edit
  • Chemical Name:(S)-N-(6-(1-amino-2-(3,5-difluorophenyl)ethyl)-2,5-dibromopyridin-3-yl)-2,2,2-trifluoroacetamide TFA salt
  • CAS No.:1620056-81-6
  • Molecular Formula:C2HF3O2*C15H10Br2F5N3O
  • Molecular Weight:617.088
  • Hs Code.:
  • Mol file:1620056-81-6.mol
(S)-N-(6-(1-amino-2-(3,5-difluorophenyl)ethyl)-2,5-dibromopyridin-3-yl)-2,2,2-trifluoroacetamide TFA salt

Synonyms:(S)-N-(6-(1-amino-2-(3,5-difluorophenyl)ethyl)-2,5-dibromopyridin-3-yl)-2,2,2-trifluoroacetamide TFA salt

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Chemical Property of (S)-N-(6-(1-amino-2-(3,5-difluorophenyl)ethyl)-2,5-dibromopyridin-3-yl)-2,2,2-trifluoroacetamide TFA salt Edit
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Technology Process of (S)-N-(6-(1-amino-2-(3,5-difluorophenyl)ethyl)-2,5-dibromopyridin-3-yl)-2,2,2-trifluoroacetamide TFA salt

There total 10 articles about (S)-N-(6-(1-amino-2-(3,5-difluorophenyl)ethyl)-2,5-dibromopyridin-3-yl)-2,2,2-trifluoroacetamide TFA salt 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 10 steps
1: sodium acetate; acetic acid / Reflux
2: selenium(IV) oxide / 1,2-dimethoxyethane / 20 h / 130 °C
3: copper(II) sulfate / dichloromethane / 2 h / 20 °C
4: copper(II) bis(trifluoromethanesulfonate) / tetrahydrofuran; dichloromethane / 1 h / 0 - 20 °C
5: hydrogenchloride / methanol; 1,4-dioxane / 0.17 h / 0 - 20 °C
6: triethylamine / dichloromethane / 0 °C
7: hydrazine hydrate / ethanol / 2 h / 20 °C
8: N-Bromosuccinimide / acetonitrile / 0.08 h / 0 °C
9: potassium carbonate / 1,4-dioxane / 0.08 h / 0 °C
10: dichloromethane / 1 h / 0 - 20 °C
With hydrogenchloride; selenium(IV) oxide; N-Bromosuccinimide; sodium acetate; copper(II) bis(trifluoromethanesulfonate); potassium carbonate; hydrazine hydrate; copper(II) sulfate; acetic acid; triethylamine; In tetrahydrofuran; 1,4-dioxane; methanol; 1,2-dimethoxyethane; ethanol; dichloromethane; acetonitrile;
Guidance literature:
Multi-step reaction with 9 steps
1: selenium(IV) oxide / 1,2-dimethoxyethane / 20 h / 130 °C
2: copper(II) sulfate / dichloromethane / 2 h / 20 °C
3: copper(II) bis(trifluoromethanesulfonate) / tetrahydrofuran; dichloromethane / 1 h / 0 - 20 °C
4: hydrogenchloride / methanol; 1,4-dioxane / 0.17 h / 0 - 20 °C
5: triethylamine / dichloromethane / 0 °C
6: hydrazine hydrate / ethanol / 2 h / 20 °C
7: N-Bromosuccinimide / acetonitrile / 0.08 h / 0 °C
8: potassium carbonate / 1,4-dioxane / 0.08 h / 0 °C
9: dichloromethane / 1 h / 0 - 20 °C
With hydrogenchloride; selenium(IV) oxide; N-Bromosuccinimide; copper(II) bis(trifluoromethanesulfonate); potassium carbonate; hydrazine hydrate; copper(II) sulfate; triethylamine; In tetrahydrofuran; 1,4-dioxane; methanol; 1,2-dimethoxyethane; ethanol; dichloromethane; acetonitrile;
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