Technology Process of C26H25F3N4O2
There total 5 articles about C26H25F3N4O2 which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
Multi-step reaction with 5 steps
1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / N,N-dimethyl-formamide
2: sodium methylate / methanol
3: 1,1'-azodicarbonyl-dipiperidine; tributylphosphine / tetrahydrofuran / 80 °C
4: hydrazine / acetonitrile
5: phosphorus pentoxide / ethanol / 80 °C
With
tributylphosphine; phosphorus pentoxide; sodium methylate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; hydrazine; 1,1'-azodicarbonyl-dipiperidine;
In
tetrahydrofuran; methanol; ethanol; N,N-dimethyl-formamide; acetonitrile;
3: |Mitsunobu Displacement;
DOI:10.1016/j.bmcl.2012.11.055
- Guidance literature:
-
Multi-step reaction with 7 steps
1: lithium hydroxide / tetrahydrofuran
2: trifluoroacetic acid
3: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / N,N-dimethyl-formamide
4: sodium methylate / methanol
5: 1,1'-azodicarbonyl-dipiperidine; tributylphosphine / tetrahydrofuran / 80 °C
6: hydrazine / acetonitrile
7: phosphorus pentoxide / ethanol / 80 °C
With
tributylphosphine; phosphorus pentoxide; sodium methylate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; trifluoroacetic acid; lithium hydroxide; hydrazine; 1,1'-azodicarbonyl-dipiperidine;
In
tetrahydrofuran; methanol; ethanol; N,N-dimethyl-formamide; acetonitrile;
1: |Wittig Olefination / 5: |Mitsunobu Displacement;
DOI:10.1016/j.bmcl.2012.11.055
- Guidance literature:
-
Multi-step reaction with 4 steps
1: sodium methylate / methanol
2: 1,1'-azodicarbonyl-dipiperidine; tributylphosphine / tetrahydrofuran / 80 °C
3: hydrazine / acetonitrile
4: phosphorus pentoxide / ethanol / 80 °C
With
tributylphosphine; phosphorus pentoxide; sodium methylate; hydrazine; 1,1'-azodicarbonyl-dipiperidine;
In
tetrahydrofuran; methanol; ethanol; acetonitrile;
2: |Mitsunobu Displacement;
DOI:10.1016/j.bmcl.2012.11.055