Technology Process of C29H32F2N4O4
There total 8 articles about C29H32F2N4O4 which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
ethyl 2-((2-((4-cyanophenoxy)methyl)-2,4-dimethyl-3,4-dihydro-2H-1,4-benzoxazin-7-yl)(3,5-difluorobenzyl)amino)acetate;
With
hydrogenchloride;
In
ethanol;
at 0 ℃;
for 0.5h;
With
ammonium acetate;
In
ethanol;
at 20 ℃;
for 24h;
DOI:10.1016/j.bmcl.2011.06.089
- Guidance literature:
-
Multi-step reaction with 5 steps
1.1: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / 48 h / Reflux
2.1: palladium on carbon; hydrogen / tetrahydrofuran / 2 h / 20 °C
3.1: sodium triacetoxyborohydride / 1,2-dichloro-ethane / 6 h / 20 °C
4.1: N-benzyl-N,N,N-triethylammonium chloride; potassium carbonate / acetonitrile / 24 h / 60 °C
5.1: hydrogenchloride / ethanol / 0.5 h / 0 °C
5.2: 24 h / 20 °C
With
hydrogenchloride; sodium triacetoxyborohydride; di-isopropyl azodicarboxylate; palladium on carbon; N-benzyl-N,N,N-triethylammonium chloride; hydrogen; potassium carbonate; triphenylphosphine;
In
tetrahydrofuran; ethanol; 1,2-dichloro-ethane; acetonitrile;
1.1: Mitsunobu reaction / 5.1: Pinner reaction / 5.2: Pinner reaction;
DOI:10.1016/j.bmcl.2011.06.089
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: palladium on carbon; hydrogen / tetrahydrofuran / 2 h / 20 °C
2.1: sodium triacetoxyborohydride / 1,2-dichloro-ethane / 6 h / 20 °C
3.1: N-benzyl-N,N,N-triethylammonium chloride; potassium carbonate / acetonitrile / 24 h / 60 °C
4.1: hydrogenchloride / ethanol / 0.5 h / 0 °C
4.2: 24 h / 20 °C
With
hydrogenchloride; sodium triacetoxyborohydride; palladium on carbon; N-benzyl-N,N,N-triethylammonium chloride; hydrogen; potassium carbonate;
In
tetrahydrofuran; ethanol; 1,2-dichloro-ethane; acetonitrile;
4.1: Pinner reaction / 4.2: Pinner reaction;
DOI:10.1016/j.bmcl.2011.06.089