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

Base Information

Chemical Name:[5-(5-amino-2-fluoro-phenyl)-5-methyl-5,6-dihydro-2H-[1,4]oxazin-3-yl]-carbamic acid tert-butyl ester
CAS No.:1429869-74-8
Molecular Formula:C₁₆H₂₂FN₃O₃
Molecular Weight:323.367
Hs Code.:

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

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

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

There total 8 articles about [5-(5-amino-2-fluoro-phenyl)-5-methyl-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: 94.0%

: 1429869-73-7
[5-(5-azido-2-fluoro-phenyl)-5-methyl-5,6-dihydro-2H-[1,4]oxazin-3-yl]-carbamic acid tert-butyl ester

: 1429869-74-8
[5-(5-amino-2-fluoro-phenyl)-5-methyl-5,6-dihydro-2H-[1,4]oxazin-3-yl]-carbamic acid tert-butyl ester

Guidance literature:: With hydrogen; In ethyl acetate; at 25 ℃; for 10h; Inert atmosphere;
DOI:10.1021/acs.jmedchem.0c02143

Reference yield:

: 1266784-13-7
rac-5-(5-bromo-2-fluorophenyl)-5-methylmorpholin-3-one

: 1429869-74-8
[5-(5-amino-2-fluoro-phenyl)-5-methyl-5,6-dihydro-2H-[1,4]oxazin-3-yl]-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: Lawessons reagent / tetrahydrofuran / 16 h / 20 °C / Reflux

2: tert.-butylhydroperoxide; ammonium hydroxide; ammonia / water; methanol / 20 °C

3: N-ethyl-N,N-diisopropylamine / dichloromethane / 0 - 20 °C

4: sodium L-ascorbate; copper(l) iodide; sodium azide; cis-N,N'-dimethyl-1,2-diaminocyclohexane / water; ethanol / 1 h / 70 °C / Inert atmosphere

5: hydrogen; palladium 10% on activated carbon / ethanol; ethyl acetate / 4.5 h / 20 °C / 75.01 Torr

With Lawessons reagent; tert.-butylhydroperoxide; ammonium hydroxide; copper(l) iodide; sodium azide; palladium 10% on activated carbon; ammonia; hydrogen; sodium L-ascorbate; N-ethyl-N,N-diisopropylamine; cis-N,N'-dimethyl-1,2-diaminocyclohexane; In tetrahydrofuran; methanol; ethanol; dichloromethane; water; ethyl acetate;

Reference yield:

: 1429869-71-5
rac-5-(5-bromo-2-fluorophenyl)-5-methylmorpholine-3-thione

: 1429869-74-8
[5-(5-amino-2-fluoro-phenyl)-5-methyl-5,6-dihydro-2H-[1,4]oxazin-3-yl]-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: tert.-butylhydroperoxide; ammonium hydroxide; ammonia / water; methanol / 20 °C

2: N-ethyl-N,N-diisopropylamine / dichloromethane / 0 - 20 °C

3: sodium L-ascorbate; copper(l) iodide; sodium azide; cis-N,N'-dimethyl-1,2-diaminocyclohexane / water; ethanol / 1 h / 70 °C / Inert atmosphere

4: hydrogen; palladium 10% on activated carbon / ethanol; ethyl acetate / 4.5 h / 20 °C / 75.01 Torr

With tert.-butylhydroperoxide; ammonium hydroxide; copper(l) iodide; sodium azide; palladium 10% on activated carbon; ammonia; hydrogen; sodium L-ascorbate; N-ethyl-N,N-diisopropylamine; cis-N,N'-dimethyl-1,2-diaminocyclohexane; In methanol; ethanol; dichloromethane; water; ethyl acetate;