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

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Chemical Name:(5-{2-fluoro-5-[(furan-2-ylmethyl)-amino]-phenyl}-5-methyl-5,6-dihydro-2H-[1,4]oxazin-3-yl)-carbamic acid tert-butyl ester
CAS No.:1429869-75-9
Molecular Formula:C₂₁H₂₆FN₃O₄
Molecular Weight:403.454
Hs Code.:

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

There total 6 articles about (5-{2-fluoro-5-[(furan-2-ylmethyl)-amino]-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:

: 98-01-1
furfural

: 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

: 1429869-75-9
(5-{2-fluoro-5-[(furan-2-ylmethyl)-amino]-phenyl}-5-methyl-5,6-dihydro-2H-[1,4]oxazin-3-yl)-carbamic acid tert-butyl ester

Guidance literature:: furfural; [5-(5-amino-2-fluoro-phenyl)-5-methyl-5,6-dihydro-2H-[1,4]oxazin-3-yl]-carbamic acid tert-butyl ester; With sodium acetate; In methanol; at 100 ℃; for 0.25h; Microwave irradiation; Inert atmosphere;

With sodium tetrahydroborate; In methanol; at 0 - 20 ℃; for 1h;

Reference yield:

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

: 1429869-75-9
(5-{2-fluoro-5-[(furan-2-ylmethyl)-amino]-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

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

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

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

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

5.1: sodium acetate / methanol / 0.25 h / 100 °C / Microwave irradiation; Inert atmosphere

5.2: 1 h / 0 - 20 °C

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

Reference yield:

: 1386997-96-1
5-(5-bromo-2-fluoro-phenyl)-5-methyl-5,6-dihydro-2H-[1,4]oxazin-3-ylamine

: 1429869-75-9
(5-{2-fluoro-5-[(furan-2-ylmethyl)-amino]-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

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

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

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

4.1: sodium acetate / methanol / 0.25 h / 100 °C / Microwave irradiation; Inert atmosphere

4.2: 1 h / 0 - 20 °C

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