[5-(5-bromo-2-fluoro-phenyl)-5-fluoromethyl-5,6-dihydro-2H-[1,4]oxazin-3-yl]-carbamic acid tert-butyl ester

Base Information

Chemical Name:[5-(5-bromo-2-fluoro-phenyl)-5-fluoromethyl-5,6-dihydro-2H-[1,4]oxazin-3-yl]-carbamic acid tert-butyl ester
CAS No.:1429869-79-3
Molecular Formula:C₁₆H₁₉BrF₂N₂O₃
Molecular Weight:405.239
Hs Code.:

Synonyms:[5-(5-bromo-2-fluoro-phenyl)-5-fluoromethyl-5,6-dihydro-2H-[1,4]oxazin-3-yl]-carbamic acid tert-butyl ester

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Chemical Property of [5-(5-bromo-2-fluoro-phenyl)-5-fluoromethyl-5,6-dihydro-2H-[1,4]oxazin-3-yl]-carbamic acid tert-butyl ester

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Technology Process of [5-(5-bromo-2-fluoro-phenyl)-5-fluoromethyl-5,6-dihydro-2H-[1,4]oxazin-3-yl]-carbamic acid tert-butyl ester

There total 9 articles about [5-(5-bromo-2-fluoro-phenyl)-5-fluoromethyl-5,6-dihydro-2H-[1,4]oxazin-3-yl]-carbamic acid tert-butyl 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:

Reference yield:

: 24424-99-5
di-tert-butyl dicarbonate

: 1429869-78-2
5-(5-bromo-2-fluoro-phenyl)-5-fluoromethyl-5,6-dihydro-2H-[1,4]oxazin-3-ylamine

: 1429869-79-3
[5-(5-bromo-2-fluoro-phenyl)-5-fluoromethyl-5,6-dihydro-2H-[1,4]oxazin-3-yl]-carbamic acid tert-butyl ester

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; at 20 ℃; for 4h; Cooling with ice;

Reference yield:

: 1262859-92-6
4-bromo-1-fluoro-2-nitromethyl-benzene

: 1429869-79-3
[5-(5-bromo-2-fluoro-phenyl)-5-fluoromethyl-5,6-dihydro-2H-[1,4]oxazin-3-yl]-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 8 steps

1: triethylamine / 1,4-dioxane / 3 h

2: acetic acid; zinc / 1 h / 40 °C

3: potassium carbonate / acetonitrile / 2 h / 35 °C

4: potassium tert-butylate; tert-butyl alcohol / 0.5 h / Reflux

5: diethylamino-sulfur trifluoride / tetrahydrofuran / 2 h

6: Lawessons reagent / tetrahydrofuran / 1 h / Reflux

7: ammonia / methanol / 15 h / 20 °C

8: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 4 h / 20 °C / Cooling with ice

With Lawessons reagent; diethylamino-sulfur trifluoride; potassium tert-butylate; ammonia; potassium carbonate; acetic acid; triethylamine; N-ethyl-N,N-diisopropylamine; zinc; tert-butyl alcohol; In tetrahydrofuran; 1,4-dioxane; methanol; acetonitrile;

Reference yield:

: 99725-12-9
4-bromo-2-(bromomethyl)-1-fluorobenzene

: 1429869-79-3
[5-(5-bromo-2-fluoro-phenyl)-5-fluoromethyl-5,6-dihydro-2H-[1,4]oxazin-3-yl]-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 9 steps

1: silver(I) nitrite / tert-butyl methyl ether / 7 h

2: triethylamine / 1,4-dioxane / 3 h

3: acetic acid; zinc / 1 h / 40 °C

4: potassium carbonate / acetonitrile / 2 h / 35 °C

5: potassium tert-butylate; tert-butyl alcohol / 0.5 h / Reflux

6: diethylamino-sulfur trifluoride / tetrahydrofuran / 2 h

7: Lawessons reagent / tetrahydrofuran / 1 h / Reflux

8: ammonia / methanol / 15 h / 20 °C

9: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 4 h / 20 °C / Cooling with ice

With Lawessons reagent; silver(I) nitrite; diethylamino-sulfur trifluoride; potassium tert-butylate; ammonia; potassium carbonate; acetic acid; triethylamine; N-ethyl-N,N-diisopropylamine; zinc; tert-butyl alcohol; In tetrahydrofuran; 1,4-dioxane; methanol; tert-butyl methyl ether; acetonitrile;